RS139648092 RELN

Health Risk Chr 7:103989218
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Associated Conditions
Norman-Roberts syndrome
Self-limited epilepsy with centrotemporal spikes
Familial temporal lobe epilepsy 7
Epilepsy
familial temporal lobe
1
Inborn genetic diseases
Norman-Roberts syndrome
Self-limited epilepsy with centrotemporal spikes
Familial temporal lobe epilepsy 7
Epilepsy
familial temporal lobe
1
Inborn genetic diseases
Other Variants in RELN
rs2117170464 rs398124191 rs144653976 rs56342240 rs115577014 rs55693709 rs141387255 rs114190729 rs200010849 rs150236371
Ask Dr. Hemsworth about this variant