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rs199473264

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473264(A;G)
Make rs199473264(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38555706
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473264
ebirs199473264
HLIrs199473264
Exacrs199473264
Varsomers199473264
Maprs199473264
PheGenIrs199473264
hapmaprs199473264
1000 genomesrs199473264
hgdprs199473264
ensemblrs199473264
gopubmedrs199473264
geneviewrs199473264
scholarrs199473264
googlers199473264
pharmgkbrs199473264
gwascentralrs199473264
openSNPrs199473264
23andMers199473264
23andMe allrs199473264
SNP Nexus

SNPshotrs199473264
SNPdbers199473264
MSV3drs199473264
GWAS Ctlgrs199473264
Max Magnitude0
ClinVar
Risk rs199473264(G;G)
Alt rs199473264(G;G)
Reference rs199473264(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38597197T>C
CLNSRC ClinVar
CLNACC RCV000058681.2,