Gene

USH1G

USH1G is a gene. This site has 11 published variants inside it and 2 near it, each from a published genetic study, joining it to 1 condition page.

Conditions it is linked to

Celiac Disease

Variants inside USH1G (11)

rs201866631 · Deafness
rs1567940507 · Hearing impairment
rs397517925 · Rare genetic deafness
rs1226851798 · Usher syndrome
rs773231689 · Usher syndrome
rs104894651 · Usher syndrome type 1G
rs104894652 · Usher syndrome type 1G
rs1316299165 · Usher syndrome type 1G
rs1337840598 · Usher syndrome type 1G
rs2544431739 · Usher syndrome type 1G
rs928656346 · Usher syndrome type 1G

Variants near USH1G (2)

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

rs148894191 · CD300LF protein levels
rs503469 · Corneal resistance factor (MTAG)

See USH1G with everything it connects to on the Gene Knowledge Graph, or as data at /api/v1/genes/USH1G.

Quoting this page

Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license

USH1G gene. MyGeneLog™. https://www.mygenelog.com/genes/USH1G

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.