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Gene

KIF1A

KIF1A is a gene. This site has 100 published variants inside it and 2 near it, each from a published genetic study, joining it to 6 condition pages.

Conditions it is linked to

• Celiac Disease
• Educational Attainment
• Height
• Hip Circumference
• Insomnia
• Kidney Function

Variants inside KIF1A (100)

• rs10196017 · AGXT protein levels
• rs10460444 · Creatinine levels
• rs146789797 · GPC1 protein levels
• rs11885091 · Height (baseline)
• rs548204329 · Hereditary spastic paraplegia
• rs786200949 · Hereditary spastic paraplegia
• rs1064794935 · Hereditary spastic paraplegia 30
• rs1064795534 · Hereditary spastic paraplegia 30
• rs1064796565 · Hereditary spastic paraplegia 30
• rs113158271 · Hereditary spastic paraplegia 30
• rs1318848388 · Hereditary spastic paraplegia 30
• rs1327297188 · Hereditary spastic paraplegia 30
• rs1469297168 · Hereditary spastic paraplegia 30
• rs1553639041 · Hereditary spastic paraplegia 30
• rs1575514086 · Hereditary spastic paraplegia 30
• rs1575637048 · Hereditary spastic paraplegia 30
• rs1575654528 · Hereditary spastic paraplegia 30
• rs2045066309 · Hereditary spastic paraplegia 30
• rs2050749062 · Hereditary spastic paraplegia 30
• rs2052419658 · Hereditary spastic paraplegia 30
• rs2054755647 · Hereditary spastic paraplegia 30
• rs2054757914 · Hereditary spastic paraplegia 30
• rs2056551129 · Hereditary spastic paraplegia 30
• rs2056552812 · Hereditary spastic paraplegia 30
• rs2125791006 · Hereditary spastic paraplegia 30
• rs2125889990 · Hereditary spastic paraplegia 30
• rs2125925871 · Hereditary spastic paraplegia 30
• rs2125976529 · Hereditary spastic paraplegia 30
• rs2125976707 · Hereditary spastic paraplegia 30
• rs2538437589 · Hereditary spastic paraplegia 30
• rs387907259 · Hereditary spastic paraplegia 30
• rs572662012 · Hereditary spastic paraplegia 30
• rs762126771 · Hereditary spastic paraplegia 30
• rs780380861 · Hereditary spastic paraplegia 30
• rs876661283 · Hereditary spastic paraplegia 30
• rs886041692 · Hereditary spastic paraplegia 30
• rs11691924 · Hip circumference adjusted for BMI
• rs4676366 · Hip circumference adjusted for BMI
• rs1057518760 · Hyperreflexia
• rs1200817308 · Inborn genetic diseases
• rs1553637932 · Inborn genetic diseases
• rs1553638309 · Inborn genetic diseases
• rs2054279545 · Inborn genetic diseases
• rs2054761091 · Inborn genetic diseases
• rs879253888 · Inborn genetic diseases
• rs4455151 · Insomnia
• rs1021122060 · Intellectual disability, autosomal dominant 9
• rs1064793161 · Intellectual disability, autosomal dominant 9
• rs1131690804 · Intellectual disability, autosomal dominant 9
• rs1131692159 · Intellectual disability, autosomal dominant 9
• rs1553638614 · Intellectual disability, autosomal dominant 9
• rs2054277617 · Intellectual disability, autosomal dominant 9
• rs2054752278 · Intellectual disability, autosomal dominant 9
• rs2055064647 · Intellectual disability, autosomal dominant 9
• rs2056558371 · Intellectual disability, autosomal dominant 9
• rs2125976585 · Intellectual disability, autosomal dominant 9
• rs2126049991 · Intellectual disability, autosomal dominant 9
• rs369692236 · Intellectual disability, autosomal dominant 9
• rs387906799 · Intellectual disability, autosomal dominant 9
• rs672601362 · Intellectual disability, autosomal dominant 9
• rs672601363 · Intellectual disability, autosomal dominant 9
• rs672601364 · Intellectual disability, autosomal dominant 9
• rs672601365 · Intellectual disability, autosomal dominant 9
• rs672601366 · Intellectual disability, autosomal dominant 9
• rs672601367 · Intellectual disability, autosomal dominant 9
• rs672601368 · Intellectual disability, autosomal dominant 9
• rs672601369 · Intellectual disability, autosomal dominant 9
• rs672601370 · Intellectual disability, autosomal dominant 9
• rs672601371 · Intellectual disability, autosomal dominant 9
• rs797045164 · Intellectual disability, autosomal dominant 9
• rs797045655 · Intellectual disability, autosomal dominant 9
• rs869312711 · Intellectual disability, autosomal dominant 9
• rs876661168 · Intellectual disability, autosomal dominant 9
• rs2537142167 · KIF1A-related disorder
• rs2538462644 · KIF1A-related disorder
• rs2126062571 · Neuropathy, hereditary sensory and autonomic, type 2A
• rs2538309390 · Neuropathy, hereditary sensory and autonomic, type 2A
• rs1057518226 · Neuropathy, hereditary sensory, type 2C
• rs1057519240 · Neuropathy, hereditary sensory, type 2C
• rs1553624714 · Neuropathy, hereditary sensory, type 2C
• rs1553633687 · Neuropathy, hereditary sensory, type 2C
• rs1553638086 · Neuropathy, hereditary sensory, type 2C
• rs1559477798 · Neuropathy, hereditary sensory, type 2C
• rs1559526692 · Neuropathy, hereditary sensory, type 2C
• rs1559527796 · Neuropathy, hereditary sensory, type 2C
• rs1575626071 · Neuropathy, hereditary sensory, type 2C
• rs2052660081 · Neuropathy, hereditary sensory, type 2C
• rs2126054153 · Neuropathy, hereditary sensory, type 2C
• rs2126071766 · Neuropathy, hereditary sensory, type 2C
• rs2536614499 · Neuropathy, hereditary sensory, type 2C
• rs2536723934 · Neuropathy, hereditary sensory, type 2C
• rs2537867758 · Neuropathy, hereditary sensory, type 2C
• rs2537927812 · Neuropathy, hereditary sensory, type 2C
• rs2538277599 · Neuropathy, hereditary sensory, type 2C
• rs2538654464 · Neuropathy, hereditary sensory, type 2C
• rs751051049 · Neuropathy, hereditary sensory, type 2C
• rs13027102 · Self-reported math ability
• rs2125874950 · Spastic paraplegia
• rs797045050 · Spastic paraplegia
• rs387906798 · Spastic paraplegia 30B, autosomal recessive

Variants near KIF1A (2)

Positions outside the gene, filed under it because it is the closest. A variant near a gene does not always act through it.

• rs11900363 · Height
• rs12614864 · Height

See KIF1A with everything it connects to on the Gene Knowledge Graph, or as data at /api/v1/genes/KIF1A.

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.