RS910498292 CASP2

Health Risk Chr 7:143291595
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Associated Conditions
Inborn genetic diseases
Intellectual developmental disorder
autosomal recessive 80
with variant lissencephaly
Inborn genetic diseases
Intellectual developmental disorder
autosomal recessive 80
with variant lissencephaly
Other Variants in CASP2
rs1801677859 rs2486983740 rs2486983838 rs1801868524 rs150852779
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