RS28999111 ACTG1

Health Risk Chr 17:81512000
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What This Variant Does
"deafness [OMIM:DEAFNESS, AUTOSOMAL DOMINANT 20]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 20
Autosomal dominant nonsyndromic hearing loss 20
Other Variants in ACTG1
rs104894544 rs104894545 rs104894546 rs28999112 rs104894547 rs267606630 rs267606631 rs281875326 rs281875325 rs11549190
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