RS267606855 GRXCR1

Health Risk Chr 4:42893495
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 25
Hearing loss
autosomal recessive
Autosomal recessive nonsyndromic hearing loss 25
Hearing loss
autosomal recessive
Other Variants in GRXCR1
rs606231120 rs146696590 rs1553941938 rs761349153 rs771844359 rs1560690591 rs569193097 rs769983282 rs774844858 rs2109812443
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