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rs199473262

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473262(A;C)
Make rs199473262(C;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position38555714
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473262
ebirs199473262
HLIrs199473262
Exacrs199473262
Varsomers199473262
Maprs199473262
PheGenIrs199473262
hapmaprs199473262
1000 genomesrs199473262
hgdprs199473262
ensemblrs199473262
gopubmedrs199473262
geneviewrs199473262
scholarrs199473262
googlers199473262
pharmgkbrs199473262
gwascentralrs199473262
openSNPrs199473262
23andMers199473262
23andMe allrs199473262
SNP Nexus

SNPshotrs199473262
SNPdbers199473262
MSV3drs199473262
GWAS Ctlgrs199473262
Max Magnitude0
ClinVar
Risk rs199473262(C;C)
Alt rs199473262(C;C)
Reference rs199473262(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome not provided
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38597205T>G
CLNSRC ClinVar
CLNACC RCV000058680.2, RCV000183079.2,