Have questions? Visit https://www.reddit.com/r/SNPedia

rs199473160

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473160(C;C)
Make rs199473160(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38587413
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473160
ebirs199473160
HLIrs199473160
Exacrs199473160
Varsomers199473160
Maprs199473160
PheGenIrs199473160
hapmaprs199473160
1000 genomesrs199473160
hgdprs199473160
ensemblrs199473160
gopubmedrs199473160
geneviewrs199473160
scholarrs199473160
googlers199473160
pharmgkbrs199473160
gwascentralrs199473160
openSNPrs199473160
23andMers199473160
23andMe allrs199473160
SNP Nexus

SNPshotrs199473160
SNPdbers199473160
MSV3drs199473160
GWAS Ctlgrs199473160
Max Magnitude0
ClinVar
Risk rs199473160(A,C;A,C)
Alt rs199473160(A,C;A,C)
Reference rs199473160(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome Long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome Long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38628904C>G; NC_000003.11:g.38628904C>T
CLNSRC ClinVar
CLNACC RCV000058499.2, RCV000171699.1,