RS104894545 ACTG1

Health Risk Chr 17:81510824
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 20
Baraitser-winter syndrome 2
Autosomal dominant nonsyndromic hearing loss 20
Baraitser-winter syndrome 2
Other Variants in ACTG1
rs28999111 rs104894544 rs104894546 rs28999112 rs104894547 rs267606630 rs267606631 rs281875326 rs281875325 rs11549190
Ask Dr. Hemsworth about this variant