Gene

ATP6V1B2

ATP6V1B2 is a gene. This site has 8 published variants inside it, each from a published genetic study.

Variants inside ATP6V1B2 (8)

rs2128886555 · ATP6V1B2 related neurodevelopmental disorders
rs794729667 · Autosomal dominant deafness - onychodystrophy syndrome
rs117853493 · High density lipoprotein cholesterol levels
rs1135401772 · Zimmermann-Laband syndrome 2
rs2486443112 · Zimmermann-Laband syndrome 2
rs2486461841 · Zimmermann-Laband syndrome 2
rs730882177 · Zimmermann-Laband syndrome 2
rs1585256207 · Zimmermann-Laband syndrome with epileptic encephalopathy

See ATP6V1B2 with everything it connects to on the Gene Knowledge Graph, or as data at /api/v1/genes/ATP6V1B2.

Quoting this page

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ATP6V1B2 gene. MyGeneLog™. https://www.mygenelog.com/genes/ATP6V1B2

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.