RS267607232 MED17

Health Risk Chr 11:93796509
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
Other Variants in MED17
rs35313315 rs587780394 rs769907044 rs116727804 rs61754525 rs745733410 rs752341132 rs548231700 rs570654786 rs1943789061
Ask Dr. Hemsworth about this variant