RS77383735 EPS8

Health Risk Chr 12:15670863
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Associated Conditions
Autosomal recessive nonsyndromic hearing loss 102
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 102
Inborn genetic diseases
Other Variants in EPS8
rs202097537 rs1945698201 rs2540431049 rs1565473322 rs773161130 rs2135847318 rs2135785787 rs2135847098 rs145722981 rs138455166
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