RS138394487 DMXL2

Health Risk Chr 15:51481071
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Associated Conditions
Inborn genetic diseases
DMXL2-related disorder
Developmental and epileptic encephalopathy
81
Polyendocrine-polyneuropathy syndrome
Hearing loss
autosomal dominant 71
Inborn genetic diseases
DMXL2-related disorder
Developmental and epileptic encephalopathy
81
Polyendocrine-polyneuropathy syndrome
Hearing loss
autosomal dominant 71
Other Variants in DMXL2
rs606231461 rs1596016716 rs754786373 rs1595955503 rs372749193 rs1595908479 rs199806210 rs182672196 rs778580507 rs1416564508
Ask Dr. Hemsworth about this variant