RS372622191 MED17

Health Risk Chr 11:93801950
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Associated Conditions
Inborn genetic diseases
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
Inborn genetic diseases
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
Other Variants in MED17
rs267607232 rs35313315 rs587780394 rs769907044 rs116727804 rs61754525 rs745733410 rs752341132 rs548231700 rs570654786
Ask Dr. Hemsworth about this variant