RS587777691 EPS8

Health Risk Chr 12:15681274
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 102
Autosomal recessive nonsyndromic hearing loss 102
Other Variants in EPS8
rs1945336251 rs1945698201 rs2540431049 rs1565473322 rs773161130 rs2135847318 rs2135785787 rs2135847098 rs145722981 rs77383735
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