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

rs199473651

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473651(G;G)
Make rs199473651(G;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175241
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473651
ebirs199473651
HLIrs199473651
Exacrs199473651
Varsomers199473651
Maprs199473651
PheGenIrs199473651
hapmaprs199473651
1000 genomesrs199473651
hgdprs199473651
ensemblrs199473651
gopubmedrs199473651
geneviewrs199473651
scholarrs199473651
googlers199473651
pharmgkbrs199473651
gwascentralrs199473651
openSNPrs199473651
23andMers199473651
23andMe allrs199473651
SNP Nexus

SNPshotrs199473651
SNPdbers199473651
MSV3drs199473651
GWAS Ctlgrs199473651
Max Magnitude0
ClinVar
Risk rs199473651(G;G)
Alt rs199473651(G;G)
Reference rs199473651(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNJ2
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000017.10:g.68171382T>G
CLNSRC ClinVar
CLNACC RCV000058296.2,