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rs199473259

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473259(C;G)
Make rs199473259(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38555735
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473259
ebirs199473259
HLIrs199473259
Exacrs199473259
Varsomers199473259
Maprs199473259
PheGenIrs199473259
hapmaprs199473259
1000 genomesrs199473259
hgdprs199473259
ensemblrs199473259
gopubmedrs199473259
geneviewrs199473259
scholarrs199473259
googlers199473259
pharmgkbrs199473259
gwascentralrs199473259
openSNPrs199473259
23andMers199473259
23andMe allrs199473259
SNP Nexus

SNPshotrs199473259
SNPdbers199473259
MSV3drs199473259
GWAS Ctlgrs199473259
Max Magnitude0
ClinVar
Risk rs199473259(G;G)
Alt rs199473259(G;G)
Reference rs199473259(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38597226G>C
CLNSRC ClinVar
CLNACC RCV000058676.2,