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rs199473218

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473218(A;A)
Make rs199473218(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38562495
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473218
ebirs199473218
HLIrs199473218
Exacrs199473218
Varsomers199473218
Maprs199473218
PheGenIrs199473218
hapmaprs199473218
1000 genomesrs199473218
hgdprs199473218
ensemblrs199473218
gopubmedrs199473218
geneviewrs199473218
scholarrs199473218
googlers199473218
pharmgkbrs199473218
gwascentralrs199473218
openSNPrs199473218
23andMers199473218
23andMe allrs199473218
SNP Nexus

SNPshotrs199473218
SNPdbers199473218
MSV3drs199473218
GWAS Ctlgrs199473218
Max Magnitude0
ClinVar
Risk rs199473218(A;A)
Alt rs199473218(A;A)
Reference rs199473218(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome not provided
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38603986C>T
CLNSRC ClinVar
CLNACC RCV000058611.2, RCV000183048.2,