RS376728796 DMXL2

Health Risk Chr 15:51500116
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Associated Conditions
Polyendocrine-polyneuropathy syndrome
Hearing loss
autosomal dominant 71
Developmental and epileptic encephalopathy
81
Inborn genetic diseases
Polyendocrine-polyneuropathy syndrome
Hearing loss
autosomal dominant 71
Developmental and epileptic encephalopathy
81
Inborn genetic diseases
Other Variants in DMXL2
rs606231461 rs1596016716 rs754786373 rs1595955503 rs372749193 rs1595908479 rs199806210 rs182672196 rs778580507 rs1416564508
Ask Dr. Hemsworth about this variant