RS797044730 ACTG1

Health Risk Chr 17:81511448
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Associated Conditions
Inborn genetic diseases
Autosomal dominant nonsyndromic hearing loss 20
Inborn genetic diseases
Autosomal dominant nonsyndromic hearing loss 20
Other Variants in ACTG1
rs28999111 rs104894544 rs104894545 rs104894546 rs28999112 rs104894547 rs267606630 rs267606631 rs281875326 rs281875325
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