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Gene

MYT1L

MYT1L is a gene. This site has 44 published variants inside it and 4 near it, each from a published genetic study, joining it to 10 condition pages.

Conditions it is linked to

• Age-Related Macular Degeneration
• Blood Pressure
• Childhood Body Mass Index
• Cognitive Decline Rate in Late MCI
• Educational Attainment
• Gut Microbiota
• Height
• Obesity and Body Weight
• Tuberculosis
• Waist Circumference

Variants inside MYT1L (44)

• rs6709211 · Body mass index
• rs7581969 · Cognitive decline rate in late mild cognitive impairment
• rs115357073 · Coprobacillus abundance in stool
• rs6755567 · Educational attainment
• rs72765564 · Gut microbiota (bacterial taxa, hurdle binary method)
• rs4553849 · Gut microbiota (functional units)
• rs2048197122 · Intellectual disability
• rs2052975031 · Intellectual disability
• rs2052976421 · Intellectual disability
• rs1057519560 · Intellectual disability, autosomal dominant 39
• rs1275489527 · Intellectual disability, autosomal dominant 39
• rs1558371790 · Intellectual disability, autosomal dominant 39
• rs1558414255 · Intellectual disability, autosomal dominant 39
• rs1573483715 · Intellectual disability, autosomal dominant 39
• rs2051764612 · Intellectual disability, autosomal dominant 39
• rs2052086981 · Intellectual disability, autosomal dominant 39
• rs2052089346 · Intellectual disability, autosomal dominant 39
• rs2052983721 · Intellectual disability, autosomal dominant 39
• rs2053737766 · Intellectual disability, autosomal dominant 39
• rs2053776375 · Intellectual disability, autosomal dominant 39
• rs2060458735 · Intellectual disability, autosomal dominant 39
• rs2149071963 · Intellectual disability, autosomal dominant 39
• rs2550356884 · Intellectual disability, autosomal dominant 39
• rs2550684752 · Intellectual disability, autosomal dominant 39
• rs2550814217 · Intellectual disability, autosomal dominant 39
• rs2550870899 · Intellectual disability, autosomal dominant 39
• rs2550898220 · Intellectual disability, autosomal dominant 39
• rs2550898327 · Intellectual disability, autosomal dominant 39
• rs2551029666 · Intellectual disability, autosomal dominant 39
• rs527880727 · Intellectual disability, autosomal dominant 39
• rs528530098 · Intellectual disability, autosomal dominant 39
• rs753426087 · Intellectual disability, autosomal dominant 39
• rs764705470 · Intellectual disability, autosomal dominant 39
• rs869320675 · Intellectual disability, autosomal dominant 39
• rs869320676 · Intellectual disability, autosomal dominant 39
• rs878853045 · Intellectual disability, autosomal dominant 39
• rs886041858 · Intellectual disability, autosomal dominant 39
• rs1258062046 · MYT1L-related neurodevelopmental disorder
• rs745333246 · Neurodevelopmental disorder
• rs4557004 · Smoking initiation
• rs12472983 · Systolic blood pressure
• rs75609205 · Tuberculosis
• rs35127888 · Waist circumference
• rs12613591 · Weight

Variants near MYT1L (4)

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

• rs10519486 · Educational attainment
• rs72771173 · Free Cholesterol to Cholesteryl Esters in Very Large HDL ratio
• rs7559111 · Height
• rs6727479 · Smoking initiation

See MYT1L with everything it connects to on the Gene Knowledge Graph, or as data at /api/v1/genes/MYT1L.

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.