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Gene

MYO7A

MYO7A is a gene. This site has 252 published variants inside it, each from a published genetic study, joining it to 3 condition pages.

Conditions it is linked to

• Celiac Disease
• Retinal Dystrophy
• Retinitis Pigmentosa

Variants inside MYO7A (252)

• rs12793619 · Aspartate aminotransferase levels
• rs3819170 · Aspartate aminotransferase levels
• rs11237123 · Aspartate aminotransferase levels (UKB data field 30650)
• rs2496745583 · Auditory neuropathy
• rs121965084 · Autosomal dominant nonsyndromic hearing loss 11
• rs1223784415 · Autosomal dominant nonsyndromic hearing loss 11
• rs1957512851 · Autosomal dominant nonsyndromic hearing loss 11
• rs2135473615 · Autosomal dominant nonsyndromic hearing loss 11
• rs750647872 · Autosomal dominant nonsyndromic hearing loss 11
• rs1057517774 · Autosomal recessive nonsyndromic hearing loss 2
• rs1057517857 · Autosomal recessive nonsyndromic hearing loss 2
• rs1060499801 · Autosomal recessive nonsyndromic hearing loss 2
• rs1060499802 · Autosomal recessive nonsyndromic hearing loss 2
• rs1060499803 · Autosomal recessive nonsyndromic hearing loss 2
• rs111033437 · Autosomal recessive nonsyndromic hearing loss 2
• rs1201586094 · Autosomal recessive nonsyndromic hearing loss 2
• rs121965081 · Autosomal recessive nonsyndromic hearing loss 2
• rs121965082 · Autosomal recessive nonsyndromic hearing loss 2
• rs1226046110 · Autosomal recessive nonsyndromic hearing loss 2
• rs1268984037 · Autosomal recessive nonsyndromic hearing loss 2
• rs1279918132 · Autosomal recessive nonsyndromic hearing loss 2
• rs1297886521 · Autosomal recessive nonsyndromic hearing loss 2
• rs1343207038 · Autosomal recessive nonsyndromic hearing loss 2
• rs1386887007 · Autosomal recessive nonsyndromic hearing loss 2
• rs1401619267 · Autosomal recessive nonsyndromic hearing loss 2
• rs1453053718 · Autosomal recessive nonsyndromic hearing loss 2
• rs1555076948 · Autosomal recessive nonsyndromic hearing loss 2
• rs1555082145 · Autosomal recessive nonsyndromic hearing loss 2
• rs1555090168 · Autosomal recessive nonsyndromic hearing loss 2
• rs1555090171 · Autosomal recessive nonsyndromic hearing loss 2
• rs1555090442 · Autosomal recessive nonsyndromic hearing loss 2
• rs1555090885 · Autosomal recessive nonsyndromic hearing loss 2
• rs1555102147 · Autosomal recessive nonsyndromic hearing loss 2
• rs1555107286 · Autosomal recessive nonsyndromic hearing loss 2
• rs1555109612 · Autosomal recessive nonsyndromic hearing loss 2
• rs1565455391 · Autosomal recessive nonsyndromic hearing loss 2
• rs1591310948 · Autosomal recessive nonsyndromic hearing loss 2
• rs1591514873 · Autosomal recessive nonsyndromic hearing loss 2
• rs1952428470 · Autosomal recessive nonsyndromic hearing loss 2
• rs1957844295 · Autosomal recessive nonsyndromic hearing loss 2
• rs2135312491 · Autosomal recessive nonsyndromic hearing loss 2
• rs2135495180 · Autosomal recessive nonsyndromic hearing loss 2
• rs2135577456 · Autosomal recessive nonsyndromic hearing loss 2
• rs2135620605 · Autosomal recessive nonsyndromic hearing loss 2
• rs2135762199 · Autosomal recessive nonsyndromic hearing loss 2
• rs2497568507 · Autosomal recessive nonsyndromic hearing loss 2
• rs2497664685 · Autosomal recessive nonsyndromic hearing loss 2
• rs267603200 · Autosomal recessive nonsyndromic hearing loss 2
• rs376535635 · Autosomal recessive nonsyndromic hearing loss 2
• rs397516292 · Autosomal recessive nonsyndromic hearing loss 2
• rs548172627 · Autosomal recessive nonsyndromic hearing loss 2
• rs564622720 · Autosomal recessive nonsyndromic hearing loss 2
• rs747656448 · Autosomal recessive nonsyndromic hearing loss 2
• rs751769391 · Autosomal recessive nonsyndromic hearing loss 2
• rs766641715 · Autosomal recessive nonsyndromic hearing loss 2
• rs1565430886 · Deafness
• rs1565469959 · Deafness
• rs746667217 · Deafness
• rs371374104 · Ear malformation
• rs530062322 · GLIPR1 protein levels
• rs1485456037 · Hearing impairment
• rs377267777 · Hearing loss, autosomal recessive
• rs1280774223 · MYO7A-related disorder
• rs1334199217 · MYO7A-related disorder
• rs1953066558 · MYO7A-related disorder
• rs1953075862 · MYO7A-related disorder
• rs1954549039 · MYO7A-related disorder
• rs1954927143 · MYO7A-related disorder
• rs1955083613 · MYO7A-related disorder
• rs1956849074 · MYO7A-related disorder
• rs1957972028 · MYO7A-related disorder
• rs2496360223 · MYO7A-related disorder
• rs2497407763 · MYO7A-related disorder
• rs2497798555 · MYO7A-related disorder
• rs373942326 · MYO7A-related disorder
• rs1555063281 · Nonsyndromic genetic hearing loss
• rs111033174 · Rare genetic deafness
• rs111033175 · Rare genetic deafness
• rs111033181 · Rare genetic deafness
• rs111033182 · Rare genetic deafness
• rs111033214 · Rare genetic deafness
• rs111033233 · Rare genetic deafness
• rs111033283 · Rare genetic deafness
• rs111033284 · Rare genetic deafness
• rs111033285 · Rare genetic deafness
• rs111033286 · Rare genetic deafness
• rs111033290 · Rare genetic deafness
• rs111033337 · Rare genetic deafness
• rs111033389 · Rare genetic deafness
• rs111033403 · Rare genetic deafness
• rs111033404 · Rare genetic deafness
• rs111033415 · Rare genetic deafness
• rs111033426 · Rare genetic deafness
• rs111033482 · Rare genetic deafness
• rs1555051455 · Rare genetic deafness
• rs199606180 · Rare genetic deafness
• rs199897298 · Rare genetic deafness
• rs2497044521 · Rare genetic deafness
• rs368657015 · Rare genetic deafness
• rs369125667 · Rare genetic deafness
• rs373169422 · Rare genetic deafness
• rs377670513 · Rare genetic deafness
• rs397516281 · Rare genetic deafness
• rs397516283 · Rare genetic deafness
• rs397516285 · Rare genetic deafness
• rs397516291 · Rare genetic deafness
• rs397516308 · Rare genetic deafness
• rs397516310 · Rare genetic deafness
• rs397516312 · Rare genetic deafness
• rs397516315 · Rare genetic deafness
• rs397516317 · Rare genetic deafness
• rs397516321 · Rare genetic deafness
• rs397516322 · Rare genetic deafness
• rs397516323 · Rare genetic deafness
• rs397516330 · Rare genetic deafness
• rs397516331 · Rare genetic deafness
• rs727504541 · Rare genetic deafness
• rs1953519454 · Retinal dystrophy
• rs1956843263 · Retinal dystrophy
• rs749747871 · Retinal dystrophy
• rs1952576456 · Retinitis pigmentosa
• rs1407313220 · Sensorineural hearing loss disorder
• rs111033195 · Usher syndrome
• rs111033486 · Usher syndrome
• rs1266443165 · Usher syndrome
• rs1353598791 · Usher syndrome
• rs1383147250 · Usher syndrome
• rs1555069337 · Usher syndrome
• rs1555090294 · Usher syndrome
• rs377640847 · Usher syndrome
• rs397516332 · Usher syndrome
• rs750358148 · Usher syndrome
• rs1060499716 · Usher syndrome type 1
• rs111033178 · Usher syndrome type 1
• rs111033180 · Usher syndrome type 1
• rs111033198 · Usher syndrome type 1
• rs111033201 · Usher syndrome type 1
• rs111033206 · Usher syndrome type 1
• rs111033215 · Usher syndrome type 1
• rs1192104600 · Usher syndrome type 1
• rs1253943370 · Usher syndrome type 1
• rs1296612982 · Usher syndrome type 1
• rs1302543317 · Usher syndrome type 1
• rs1307924861 · Usher syndrome type 1
• rs1403288739 · Usher syndrome type 1
• rs1461201353 · Usher syndrome type 1
• rs1472566324 · Usher syndrome type 1
• rs1555064033 · Usher syndrome type 1
• rs1555067598 · Usher syndrome type 1
• rs1555067667 · Usher syndrome type 1
• rs1555069238 · Usher syndrome type 1
• rs1555082994 · Usher syndrome type 1
• rs1565397890 · Usher syndrome type 1
• rs1951308166 · Usher syndrome type 1
• rs1952434877 · Usher syndrome type 1
• rs1952585733 · Usher syndrome type 1
• rs1954248090 · Usher syndrome type 1
• rs1956759935 · Usher syndrome type 1
• rs1956938352 · Usher syndrome type 1
• rs1957642707 · Usher syndrome type 1
• rs1957842461 · Usher syndrome type 1
• rs1957902751 · Usher syndrome type 1
• rs1957904821 · Usher syndrome type 1
• rs201892914 · Usher syndrome type 1
• rs2135244325 · Usher syndrome type 1
• rs2135244869 · Usher syndrome type 1
• rs2135465268 · Usher syndrome type 1
• rs2135682219 · Usher syndrome type 1
• rs2135712224 · Usher syndrome type 1
• rs2135804929 · Usher syndrome type 1
• rs2496748155 · Usher syndrome type 1
• rs2496843802 · Usher syndrome type 1
• rs2497276257 · Usher syndrome type 1
• rs2497634855 · Usher syndrome type 1
• rs376764423 · Usher syndrome type 1
• rs397516295 · Usher syndrome type 1
• rs530700420 · Usher syndrome type 1
• rs548381313 · Usher syndrome type 1
• rs727503329 · Usher syndrome type 1
• rs755934966 · Usher syndrome type 1
• rs760292207 · Usher syndrome type 1
• rs121965079 · Usher syndrome type 1B
• rs121965080 · Usher syndrome type 1B
• rs121965083 · Usher syndrome type 1B
• rs121965085 · Usher syndrome type 1B
• rs1236207116 · Usher syndrome type 1B
• rs1291827891 · Usher syndrome type 1B
• rs1453718975 · Usher syndrome type 1B
• rs1474868859 · Usher syndrome type 1B
• rs1555105118 · Usher syndrome type 1B
• rs1952694662 · Usher syndrome type 1B
• rs2135310334 · Usher syndrome type 1B
• rs2135494876 · Usher syndrome type 1B
• rs28934610 · Usher syndrome type 1B
• rs35689081 · Usher syndrome type 1B
• rs397516325 · Usher syndrome type 1B
• rs41298133 · Usher syndrome type 1B
• rs752388932 · Usher syndrome type 1B
• rs761469964 · Usher syndrome type 1B
• rs1954240719 · Usher syndrome type 2

Showing 200 of 252. Search for all of them.

See MYO7A with everything it connects to on the Gene Knowledge Graph, or as data at /api/v1/genes/MYO7A.

A gene page gathers published research; it is not a test result and not medical advice. If a gene matters to your health, talk to a doctor or a genetic counsellor.