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rs199473277

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473277(C;C)
Make rs199473277(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38554311
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473277
ebirs199473277
HLIrs199473277
Exacrs199473277
Varsomers199473277
Maprs199473277
PheGenIrs199473277
hapmaprs199473277
1000 genomesrs199473277
hgdprs199473277
ensemblrs199473277
gopubmedrs199473277
geneviewrs199473277
scholarrs199473277
googlers199473277
pharmgkbrs199473277
gwascentralrs199473277
openSNPrs199473277
23andMers199473277
23andMe allrs199473277
SNP Nexus

SNPshotrs199473277
SNPdbers199473277
MSV3drs199473277
GWAS Ctlgrs199473277
Max Magnitude0
ClinVar
Risk rs199473277(C;C)
Alt rs199473277(C;C)
Reference rs199473277(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38595802A>G
CLNSRC ClinVar
CLNACC RCV000058704.2,