RS202138002 P2RX2

Health Risk Chr 12:132621535
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 41
Autosomal dominant nonsyndromic hearing loss 41
Autosomal dominant nonsyndromic hearing loss 41
Autosomal dominant nonsyndromic hearing loss 41
Other Variants in P2RX2
rs587777692 rs199712315 rs115260724 rs150293706 rs199955493 rs200978001 rs369100205 rs775460016 rs143626910 rs369473481
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