RS200818171 MYH14

Health Risk Chr 19:50223085
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 4A
Inborn genetic diseases
Autosomal dominant nonsyndromic hearing loss 4A
Inborn genetic diseases
Other Variants in MYH14
rs119103279 rs28940307 rs119103280 rs119103281 rs113993956 rs142696359 rs397516628 rs397516629 rs200272339 rs200878464
Ask Dr. Hemsworth about this variant