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rs199473263

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473263(C;C)
Make rs199473263(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38555705
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473263
ebirs199473263
HLIrs199473263
Exacrs199473263
Varsomers199473263
Maprs199473263
PheGenIrs199473263
hapmaprs199473263
1000 genomesrs199473263
hgdprs199473263
ensemblrs199473263
gopubmedrs199473263
geneviewrs199473263
scholarrs199473263
googlers199473263
pharmgkbrs199473263
gwascentralrs199473263
openSNPrs199473263
23andMers199473263
23andMe allrs199473263
SNP Nexus

SNPshotrs199473263
SNPdbers199473263
MSV3drs199473263
GWAS Ctlgrs199473263
Max Magnitude0
ClinVar
Risk rs199473263(C;C)
Alt rs199473263(C;C)
Reference rs199473263(T;T)
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.38597196A>G
CLNSRC ClinVar
CLNACC RCV000058682.2, RCV000183196.2,