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rs199473372

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473372(G;T)
Make rs199473372(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175271
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473372
ebirs199473372
HLIrs199473372
Exacrs199473372
Varsomers199473372
Maprs199473372
PheGenIrs199473372
hapmaprs199473372
1000 genomesrs199473372
hgdprs199473372
ensemblrs199473372
gopubmedrs199473372
geneviewrs199473372
scholarrs199473372
googlers199473372
pharmgkbrs199473372
gwascentralrs199473372
openSNPrs199473372
23andMers199473372
23andMe allrs199473372
SNP Nexus

SNPshotrs199473372
SNPdbers199473372
MSV3drs199473372
GWAS Ctlgrs199473372
Max Magnitude0
ClinVar
Risk rs199473372(T;T)
Alt rs199473372(T;T)
Reference rs199473372(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNJ2
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000017.10:g.68171412G>T
CLNSRC ClinVar
CLNACC RCV000058303.2,