Gene

MED12L

MED12L is a gene. This site has 18 published variants inside it, each from a published genetic study, joining it to 5 condition pages.

Conditions it is linked to

Variants inside MED12L (18)

rs1472121 · Alanine aminotransferase levels
rs8180086 · APP protein levels
rs13088531 · CBLIF protein levels
rs77277933 · CCL14 protein levels
rs1756333400 · Inborn genetic diseases
rs1231521 · Insomnia
rs1560108090 · Intellectual disability
rs1466684 · Monocyte count
rs1560069336 · Nizon-Isidor syndrome
rs1724263784 · Nizon-Isidor syndrome
rs2149096532 · Nizon-Isidor syndrome
rs2473757305 · Nizon-Isidor syndrome
rs6803771 · Parkinson's disease
rs11707416 · Parkinson's disease or first degree relation to individual with Parkinson's disease
rs6803224 · Platelet side scatter distribution width
rs114050142 · Smoking initiation
rs2276764 · Total bilirubin levels
rs4146770 · white blood cell count (WBC, mean, inv-norm transformed)

See MED12L with everything it connects to on the Gene Knowledge Graph, or as data at /api/v1/genes/MED12L.

Quoting this page

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MED12L gene. MyGeneLog™. https://www.mygenelog.com/genes/MED12L

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.