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rs199473068

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473068(C;G)
Make rs199473068(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38620886
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473068
ebirs199473068
HLIrs199473068
Exacrs199473068
Varsomers199473068
Maprs199473068
PheGenIrs199473068
hapmaprs199473068
1000 genomesrs199473068
hgdprs199473068
ensemblrs199473068
gopubmedrs199473068
geneviewrs199473068
scholarrs199473068
googlers199473068
pharmgkbrs199473068
gwascentralrs199473068
openSNPrs199473068
23andMers199473068
23andMe allrs199473068
SNP Nexus

SNPshotrs199473068
SNPdbers199473068
MSV3drs199473068
GWAS Ctlgrs199473068
Max Magnitude0
ClinVar
Risk rs199473068(G,T;G,T)
Alt rs199473068(G,T;G,T)
Reference rs199473068(C;C)
Significance Other
Disease Congenital long QT syndrome not specified
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome not specified
Reversed 1
HGVS NC_000003.11:g.38662377G>C
CLNSRC ClinVar
CLNACC RCV000058798.2, RCV000157477.3,