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rs45514691

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45514691(C;T)
Make rs45514691(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38554345
GeneSCN5A
is asnp
is mentioned by
dbSNPrs45514691
ebirs45514691
HLIrs45514691
Exacrs45514691
Varsomers45514691
Maprs45514691
PheGenIrs45514691
hapmaprs45514691
1000 genomesrs45514691
hgdprs45514691
ensemblrs45514691
gopubmedrs45514691
geneviewrs45514691
scholarrs45514691
googlers45514691
pharmgkbrs45514691
gwascentralrs45514691
openSNPrs45514691
23andMers45514691
23andMe allrs45514691
SNP Nexus

SNPshotrs45514691
SNPdbers45514691
MSV3drs45514691
GWAS Ctlgrs45514691
Max Magnitude0
ClinVar
Risk rs45514691(T;T)
Alt rs45514691(T;T)
Reference rs45514691(C;C)
Significance Pathogenic
Disease Brugada syndrome not specified not provided
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not specified not provided
Reversed 1
HGVS NC_000003.11:g.38595836G>A
CLNSRC ClinVar
CLNACC RCV000058701.2, RCV000154836.1, RCV000183082.2,