RS368472938 MYH14

Health Risk Chr 19:50247037
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Associated Conditions
Inborn genetic diseases
Autosomal dominant nonsyndromic hearing loss 4A
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome
Inborn genetic diseases
Autosomal dominant nonsyndromic hearing loss 4A
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome
Other Variants in MYH14
rs119103279 rs28940307 rs119103280 rs119103281 rs113993956 rs142696359 rs397516628 rs397516629 rs200272339 rs200878464
Ask Dr. Hemsworth about this variant