RS1060499797 GPSM2

Health Risk Chr 1:108903149
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hearing loss
autosomal recessive
Chudley-McCullough syndrome
Hearing loss
autosomal recessive
Chudley-McCullough syndrome
Other Variants in GPSM2
rs267606854 rs387907010 rs528069912 rs145191476 rs777695770 rs61754640 rs140949805 rs79730689 rs199575734 rs727505300
Ask Dr. Hemsworth about this variant