RS362800 RELN

Health Risk Chr 7:103565288
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Associated Conditions
Norman-Roberts syndrome
Familial temporal lobe epilepsy 7
Lissencephaly
Inborn genetic diseases
Norman-Roberts syndrome
Familial temporal lobe epilepsy 7
Lissencephaly
Inborn genetic diseases
Other Variants in RELN
rs2117170464 rs139648092 rs398124191 rs144653976 rs56342240 rs115577014 rs55693709 rs141387255 rs114190729 rs200010849
Ask Dr. Hemsworth about this variant