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rs199473276

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473276(C;G)
Make rs199473276(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38554313
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473276
ebirs199473276
HLIrs199473276
Exacrs199473276
Varsomers199473276
Maprs199473276
PheGenIrs199473276
hapmaprs199473276
1000 genomesrs199473276
hgdprs199473276
ensemblrs199473276
gopubmedrs199473276
geneviewrs199473276
scholarrs199473276
googlers199473276
pharmgkbrs199473276
gwascentralrs199473276
openSNPrs199473276
23andMers199473276
23andMe allrs199473276
SNP Nexus

SNPshotrs199473276
SNPdbers199473276
MSV3drs199473276
GWAS Ctlgrs199473276
Max Magnitude0
ClinVar
Risk rs199473276(G;G)
Alt rs199473276(G;G)
Reference rs199473276(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38595804G>C
CLNSRC ClinVar
CLNACC RCV000058703.2,