RS267606631 ACTG1

Health Risk Chr 17:81511269
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 20
Rare genetic deafness
Hearing impairment
Baraitser-winter syndrome 2
Autosomal dominant nonsyndromic hearing loss 20
Rare genetic deafness
Hearing impairment
Baraitser-winter syndrome 2
Other Variants in ACTG1
rs28999111 rs104894544 rs104894545 rs104894546 rs28999112 rs104894547 rs267606630 rs281875326 rs281875325 rs11549190
Ask Dr. Hemsworth about this variant