Have questions? Visit https://www.reddit.com/r/SNPedia

rs150264233

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150264233(A;A)
Make rs150264233(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position38550661
GeneSCN5A
is asnp
is mentioned by
dbSNPrs150264233
ebirs150264233
HLIrs150264233
Exacrs150264233
Varsomers150264233
Maprs150264233
PheGenIrs150264233
hapmaprs150264233
1000 genomesrs150264233
hgdprs150264233
ensemblrs150264233
gopubmedrs150264233
geneviewrs150264233
scholarrs150264233
googlers150264233
pharmgkbrs150264233
gwascentralrs150264233
openSNPrs150264233
23andMers150264233
23andMe allrs150264233
SNP Nexus

SNPshotrs150264233
SNPdbers150264233
MSV3drs150264233
GWAS Ctlgrs150264233
Max Magnitude0
ClinVar
Risk rs150264233(A;A)
Alt rs150264233(A;A)
Reference rs150264233(G;G)
Significance Pathogenic
Disease not specified not provided Long QT syndrome Death in infancy
Variation info
Gene SCN5A
CLNDBN not specified not provided Long QT syndrome Death in infancy
Reversed 0
HGVS NC_000003.11:g.38592152G>A
CLNSRC
CLNACC RCV000041630.2, RCV000058802.4, RCV000148839.1, RCV000234983.1,