RS948962 MYO7A

Health Risk Chr 11:77208432 snv missense variant

Upload your DNA to see your genotype for this variant.

What This Variant Does

"CLNSIG=2

Associated Conditions

Usher syndrome type 1B

GWAS Studies (1)

Trait	Risk Allele	OR / Beta	P-value	Study
Aspartate aminotransferase (AST, minimum, inv-norm transformed)	C	β: 0.018	4E-12	PubMed

Population Frequencies

gnomAD ALL

53.6%

1kG AFR

24.3%

1kG ALL

50.1%

1kG AMR

54.9%

1kG EAS

33.4%

1kG EUR

50%

1kG SAS

28.3%

Other Variants in MYO7A