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rs199473202

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473202(A;C)
Make rs199473202(C;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position38575367
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473202
ebirs199473202
HLIrs199473202
Exacrs199473202
Varsomers199473202
Maprs199473202
PheGenIrs199473202
hapmaprs199473202
1000 genomesrs199473202
hgdprs199473202
ensemblrs199473202
gopubmedrs199473202
geneviewrs199473202
scholarrs199473202
googlers199473202
pharmgkbrs199473202
gwascentralrs199473202
openSNPrs199473202
23andMers199473202
23andMe allrs199473202
SNP Nexus

SNPshotrs199473202
SNPdbers199473202
MSV3drs199473202
GWAS Ctlgrs199473202
Max Magnitude0
ClinVar
Risk rs199473202(C;C)
Alt rs199473202(C;C)
Reference rs199473202(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.38616858T>G
CLNSRC ClinVar
CLNACC RCV000058580.2,