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rs199473327

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473327(A;A)
Make rs199473327(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38550634
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473327
ebirs199473327
HLIrs199473327
Exacrs199473327
Varsomers199473327
Maprs199473327
PheGenIrs199473327
hapmaprs199473327
1000 genomesrs199473327
hgdprs199473327
ensemblrs199473327
gopubmedrs199473327
geneviewrs199473327
scholarrs199473327
googlers199473327
pharmgkbrs199473327
gwascentralrs199473327
openSNPrs199473327
23andMers199473327
23andMe allrs199473327
SNP Nexus

SNPshotrs199473327
SNPdbers199473327
MSV3drs199473327
GWAS Ctlgrs199473327
Max Magnitude0
ClinVar
Risk rs199473327(A;A)
Alt rs199473327(A;A)
Reference rs199473327(G;G)
Significance Pathogenic
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.38592125C>T
CLNSRC ClinVar
CLNACC RCV000058804.2, RCV000183104.2,