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rs199473064

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473064(G;G)
Make rs199473064(G;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38620926
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473064
ebirs199473064
HLIrs199473064
Exacrs199473064
Varsomers199473064
Maprs199473064
PheGenIrs199473064
hapmaprs199473064
1000 genomesrs199473064
hgdprs199473064
ensemblrs199473064
gopubmedrs199473064
geneviewrs199473064
scholarrs199473064
googlers199473064
pharmgkbrs199473064
gwascentralrs199473064
openSNPrs199473064
23andMers199473064
23andMe allrs199473064
SNP Nexus

SNPshotrs199473064
SNPdbers199473064
MSV3drs199473064
GWAS Ctlgrs199473064
Max Magnitude0
ClinVar
Risk rs199473064(G;G)
Alt rs199473064(G;G)
Reference rs199473064(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.38662417A>C
CLNSRC ClinVar
CLNACC RCV000058761.2,