RS397514608 OTOG

Health Risk Chr 11:17613696
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 18B
Autosomal recessive nonsyndromic hearing loss 18B
Other Variants in OTOG
rs1029389440 rs397514607 rs183470913 rs191662816 rs545257884 rs552304627 rs876657657 rs61978648 rs191354103 rs876657936
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