RS41269323 MYO6

Health Risk Chr 6:75914821
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 37
Autosomal dominant nonsyndromic hearing loss 22
Autosomal recessive nonsyndromic hearing loss 37
Autosomal dominant nonsyndromic hearing loss 22
GWAS Studies (2)
Trait Risk Allele OR / Beta P-value Study
Unconventional myosin-VI levels A OR: 0.62 4E-22 PubMed
Unconventional myosin-VI levels A OR: 0.79 1E-15 PubMed
Other Variants in MYO6
rs121912557 rs1562201376 rs121912558 rs121912559 rs121912560 rs121912561 rs1562283089 rs199798449 rs144031818 rs111033431
Ask Dr. Hemsworth about this variant