RS876657688 EDNRB

Health Risk Chr 13:77903339
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Rare genetic deafness
Other Variants in EDNRB
rs104894387 rs104894388 rs104894389 rs769735757 rs1801710 rs5352 rs104894390 rs104894391 rs267606780 rs2070591
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