RS104894547 ACTG1

Health Risk Chr 17:81510709
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 20
Autosomal dominant nonsyndromic hearing loss 20
Other Variants in ACTG1
rs28999111 rs104894544 rs104894545 rs104894546 rs28999112 rs267606630 rs267606631 rs281875326 rs281875325 rs11549190
Ask Dr. Hemsworth about this variant