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rs199473057

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473057(A;G)
Make rs199473057(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38630360
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473057
ebirs199473057
HLIrs199473057
Exacrs199473057
Varsomers199473057
Maprs199473057
PheGenIrs199473057
hapmaprs199473057
1000 genomesrs199473057
hgdprs199473057
ensemblrs199473057
gopubmedrs199473057
geneviewrs199473057
scholarrs199473057
googlers199473057
pharmgkbrs199473057
gwascentralrs199473057
openSNPrs199473057
23andMers199473057
23andMe allrs199473057
SNP Nexus

SNPshotrs199473057
SNPdbers199473057
MSV3drs199473057
GWAS Ctlgrs199473057
Max Magnitude0
ClinVar
Risk rs199473057(G;G)
Alt rs199473057(G;G)
Reference rs199473057(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.38671851T>C
CLNSRC ClinVar
CLNACC RCV000058572.2,