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rs199473155

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473155(A;T)
Make rs199473155(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38587561
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473155
ebirs199473155
HLIrs199473155
Exacrs199473155
Varsomers199473155
Maprs199473155
PheGenIrs199473155
hapmaprs199473155
1000 genomesrs199473155
hgdprs199473155
ensemblrs199473155
gopubmedrs199473155
geneviewrs199473155
scholarrs199473155
googlers199473155
pharmgkbrs199473155
gwascentralrs199473155
openSNPrs199473155
23andMers199473155
23andMe allrs199473155
SNP Nexus

SNPshotrs199473155
SNPdbers199473155
MSV3drs199473155
GWAS Ctlgrs199473155
Max Magnitude0
ClinVar
Risk rs199473155(G;G)
Alt rs199473155(G;G)
Reference rs199473155(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.38629052T>A
CLNSRC ClinVar
CLNACC RCV000058493.2,