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rs199473652

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473652(A;G)
Make rs199473652(G;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175259
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473652
ebirs199473652
HLIrs199473652
Exacrs199473652
Varsomers199473652
Maprs199473652
PheGenIrs199473652
hapmaprs199473652
1000 genomesrs199473652
hgdprs199473652
ensemblrs199473652
gopubmedrs199473652
geneviewrs199473652
scholarrs199473652
googlers199473652
pharmgkbrs199473652
gwascentralrs199473652
openSNPrs199473652
23andMers199473652
23andMe allrs199473652
SNP Nexus

SNPshotrs199473652
SNPdbers199473652
MSV3drs199473652
GWAS Ctlgrs199473652
Max Magnitude0
ClinVar
Risk rs199473652(G;G)
Alt rs199473652(G;G)
Reference rs199473652(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNJ2
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000017.10:g.68171400A>G
CLNSRC ClinVar
CLNACC RCV000058299.2,