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Gene

KCNQ5

KCNQ5 is a gene. This site has 41 published variants inside it, each from a published genetic study, joining it to 8 condition pages.

Conditions it is linked to

• Blood Pressure
• Celiac Disease
• Childhood Body Mass Index
• Depression (Self-Reported Symptoms)
• Height
• Insomnia
• Myopia
• Obesity and Body Weight

Variants inside KCNQ5 (41)

• rs76454399 · Bioavailable testosterone levels
• rs111232109 · Body mass index
• rs111305382 · Body mass index
• rs111600783 · Body mass index
• rs111685356 · Body mass index
• rs111893880 · Body mass index
• rs112094298 · Body mass index
• rs112997141 · Body mass index
• rs113572243 · Body mass index
• rs113727718 · Body mass index
• rs113813394 · Body mass index
• rs115475489 · Body mass index
• rs116718231 · Body mass index
• rs150792064 · Body mass index
• rs75298955 · Body mass index
• rs75673421 · Body mass index
• rs76951078 · Body mass index
• rs77217482 · Body mass index
• rs77661114 · Body mass index
• rs77912034 · Body mass index
• rs78764796 · Body mass index
• rs79117867 · Body mass index
• rs947612 · Body mass index
• rs9446841 · CD109 protein levels
• rs112348907 · Depression (broad)
• rs185203365 · GLIPR1 protein levels
• rs17742423 · Height
• rs4582343 · Height
• rs1135401955 · Inborn genetic diseases
• rs1554210415 · Inborn genetic diseases
• rs1554210418 · Inborn genetic diseases
• rs9342993 · Insomnia
• rs1554201137 · Intellectual disability, autosomal dominant 46
• rs1765561142 · Intellectual disability, autosomal dominant 46
• rs1775232605 · Intellectual disability, autosomal dominant 46
• rs9360621 · Lung function (FEV1/FVC)
• rs529978709 · Open wound of hand except finger(s) (PheCode 871.1)
• rs13206405 · Peak expiratory flow
• rs1891394 · Refractive error
• rs7775087 · Refractive error
• rs12214158 · Systolic blood pressure

See KCNQ5 with everything it connects to on the Gene Knowledge Graph, or as data at /api/v1/genes/KCNQ5.

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.