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rs199473260

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473260(A;G)
Make rs199473260(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38555720
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473260
ebirs199473260
HLIrs199473260
Exacrs199473260
Varsomers199473260
Maprs199473260
PheGenIrs199473260
hapmaprs199473260
1000 genomesrs199473260
hgdprs199473260
ensemblrs199473260
gopubmedrs199473260
geneviewrs199473260
scholarrs199473260
googlers199473260
pharmgkbrs199473260
gwascentralrs199473260
openSNPrs199473260
23andMers199473260
23andMe allrs199473260
SNP Nexus

SNPshotrs199473260
SNPdbers199473260
MSV3drs199473260
GWAS Ctlgrs199473260
Max Magnitude0
ClinVar
Risk rs199473260(G;G)
Alt rs199473260(G;G)
Reference rs199473260(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome Atrial fibrillation
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome Atrial fibrillation
Reversed 1
HGVS NC_000003.11:g.38597211T>C
CLNSRC ClinVar
CLNACC RCV000058678.2, RCV000171569.1,