RS114190729 RELN

Health Risk Chr 7:103557062 snv missense variant
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Associated Conditions
Norman-Roberts syndrome
Familial temporal lobe epilepsy 7
Epilepsy
familial temporal lobe
1
Inborn genetic diseases
Norman-Roberts syndrome
Familial temporal lobe epilepsy 7
Epilepsy
familial temporal lobe
1
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0.1%
1kG AFR
100%
1kG ALL
0.1%
1kG AMR
99.9%
1kG EAS
100%
1kG EUR
99.8%
1kG SAS
100%
Other Variants in RELN
rs2117170464 rs139648092 rs398124191 rs144653976 rs56342240 rs115577014 rs55693709 rs141387255 rs200010849 rs150236371
Ask Dr. Hemsworth about this variant