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rs199473390

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473390(G;T)
Make rs199473390(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position70176304
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473390
ebirs199473390
HLIrs199473390
Exacrs199473390
Varsomers199473390
Maprs199473390
PheGenIrs199473390
hapmaprs199473390
1000 genomesrs199473390
hgdprs199473390
ensemblrs199473390
gopubmedrs199473390
geneviewrs199473390
scholarrs199473390
googlers199473390
pharmgkbrs199473390
gwascentralrs199473390
openSNPrs199473390
23andMers199473390
23andMe allrs199473390
SNP Nexus

SNPshotrs199473390
SNPdbers199473390
MSV3drs199473390
GWAS Ctlgrs199473390
Max Magnitude0
ClinVar
Risk rs199473390(A,C,T;A,C,T)
Alt rs199473390(A,C,T;A,C,T)
Reference rs199473390(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.68172445G>T
CLNSRC ClinVar
CLNACC RCV000058292.2,