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rs3918389

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3918389(C;C)
Make rs3918389(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38603948
GeneSCN5A
is asnp
is mentioned by
dbSNPrs3918389
ebirs3918389
HLIrs3918389
Exacrs3918389
Varsomers3918389
Maprs3918389
PheGenIrs3918389
hapmaprs3918389
1000 genomesrs3918389
hgdprs3918389
ensemblrs3918389
gopubmedrs3918389
geneviewrs3918389
scholarrs3918389
googlers3918389
pharmgkbrs3918389
gwascentralrs3918389
openSNPrs3918389
23andMers3918389
23andMe allrs3918389
SNP Nexus

SNPshotrs3918389
SNPdbers3918389
MSV3drs3918389
GWAS Ctlgrs3918389
Max Magnitude0
? (C;C) (C;G) (G;G) 28
ClinVar
Risk rs3918389(A,C,T;A,C,T)
Alt rs3918389(A,C,T;A,C,T)
Reference rs3918389(G;G)
Significance Pathogenic
Disease not specified Brugada syndrome
Variation info
Gene SCN5A
CLNDBN not specified Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38645439C>A; NC_000003.11:g.38645439C>T
CLNSRC ClinVar
CLNACC RCV000182981.2, RCV000058438.2,