RS762352115 MARVELD2

Health Risk Chr 5:69432676
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 49
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 49
Rare genetic deafness
Other Variants in MARVELD2
rs200781822 rs1174369347 rs118203957 rs61736168 rs150773481 rs140764671 rs139854607 rs138680809 rs727503157 rs72773422
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