RS138909076 RELN

Health Risk Chr 7:103551198 snv missense variant

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Associated Conditions

Norman-Roberts syndrome

Familial temporal lobe epilepsy 7

Inborn genetic diseases

Norman-Roberts syndrome

Familial temporal lobe epilepsy 7

Inborn genetic diseases

Population Frequencies

gnomAD ALL

100%

1kG AFR

100%

1kG ALL

100%

1kG AMR

0.1%

1kG EAS

100%

1kG EUR

99.9%

1kG SAS

100%

Other Variants in RELN