RS587777424 GRXCR2

Health Risk Chr 5:145859765
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 101
Autosomal recessive nonsyndromic hearing loss 101
Other Variants in GRXCR2
rs151087704 rs773457218 rs1756441567 rs770833599
Ask Dr. Hemsworth about this variant