RS137852839 WHRN

Health Risk Chr 9:114403982
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 31
Usher syndrome
Usher syndrome type 2D
Autosomal recessive nonsyndromic hearing loss 31
Usher syndrome
Usher syndrome type 2D
Other Variants in WHRN
rs137852840 rs2133130286 rs1589229634 rs1306987034 rs56059137 rs149558159 rs397517255 rs200377723 rs370178817 rs111033459
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