RS1044396 CHRNA4

Health Risk Chr 20:63349781 snv missense variant

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What This Variant Does

"associated with vulnerability to nicotine addiction in men. g2b2mh blog rs1044396 mediates effects o...

Associated Conditions

Autosomal dominant nocturnal frontal lobe epilepsy

ClinVar Assertions (1)

NM_000744.7(CHRNA4):c.1629C>T (p.Ser543=)

· 12 submitters

Population Frequencies

gnomAD ALL

52.3%

1kG AFR

93.9%

1kG ALL

32.3%

1kG AMR

49%

1kG EAS

26.8%

1kG EUR

52.9%

1kG SAS

59.4%

Other Variants in CHRNA4