RS1555666715 ACTG1

Health Risk Chr 17:81511373
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Associated Conditions
Rare genetic deafness
Baraitser-winter syndrome 2
Autosomal dominant nonsyndromic hearing loss 20
Rare genetic deafness
Baraitser-winter syndrome 2
Autosomal dominant nonsyndromic hearing loss 20
Other Variants in ACTG1
rs28999111 rs104894544 rs104894545 rs104894546 rs28999112 rs104894547 rs267606630 rs267606631 rs281875326 rs281875325
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