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rs199473226

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473226(A;G)
Make rs199473226(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38560392
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473226
ebirs199473226
HLIrs199473226
Exacrs199473226
Varsomers199473226
Maprs199473226
PheGenIrs199473226
hapmaprs199473226
1000 genomesrs199473226
hgdprs199473226
ensemblrs199473226
gopubmedrs199473226
geneviewrs199473226
scholarrs199473226
googlers199473226
pharmgkbrs199473226
gwascentralrs199473226
openSNPrs199473226
23andMers199473226
23andMe allrs199473226
SNP Nexus

SNPshotrs199473226
SNPdbers199473226
MSV3drs199473226
GWAS Ctlgrs199473226
Max Magnitude0
ClinVar
Risk rs199473226(G;G)
Alt rs199473226(G;G)
Reference rs199473226(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.38601883T>C
CLNSRC ClinVar
CLNACC RCV000058626.2, RCV000183057.2,