FAM136A Chromosome 2

1 variant 1 Health Risk

Upload your DNA to see your personal genotypes for variants in FAM136A.

What This Gene Does
"CLNSIG=5
Associated Conditions (1)
Meniere disease
Key Variants
RS690016537
Pathogenic
Meniere disease, Meniere disease
Health Risk
All Variants (1)
RSID Category Clinical Significance Conditions
RS690016537 Health Risk Pathogenic Meniere disease, Meniere disease
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