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rs79299226

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs79299226(C;C)
Make rs79299226(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38550898
GeneSCN5A
is asnp
is mentioned by
dbSNPrs79299226
ebirs79299226
HLIrs79299226
Exacrs79299226
Varsomers79299226
Maprs79299226
PheGenIrs79299226
hapmaprs79299226
1000 genomesrs79299226
hgdprs79299226
ensemblrs79299226
gopubmedrs79299226
geneviewrs79299226
scholarrs79299226
googlers79299226
pharmgkbrs79299226
gwascentralrs79299226
openSNPrs79299226
23andMers79299226
23andMe allrs79299226
SNP Nexus

SNPshotrs79299226
SNPdbers79299226
MSV3drs79299226
GWAS Ctlgrs79299226
Max Magnitude0
ClinVar
Risk rs79299226(C;C)
Alt rs79299226(C;C)
Reference rs79299226(T;T)
Significance Pathogenic
Disease Acquired long QT syndrome
Variation info
Gene SCN5A
CLNDBN Acquired long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38592389A>G
CLNSRC ClinVar
CLNACC RCV000058784.2,