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rs199473368

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473368(A;A)
Make rs199473368(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175239
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473368
ebirs199473368
HLIrs199473368
Exacrs199473368
Varsomers199473368
Maprs199473368
PheGenIrs199473368
hapmaprs199473368
1000 genomesrs199473368
hgdprs199473368
ensemblrs199473368
gopubmedrs199473368
geneviewrs199473368
scholarrs199473368
googlers199473368
pharmgkbrs199473368
gwascentralrs199473368
openSNPrs199473368
23andMers199473368
23andMe allrs199473368
SNP Nexus

SNPshotrs199473368
SNPdbers199473368
MSV3drs199473368
GWAS Ctlgrs199473368
Max Magnitude0
ClinVar
Risk rs199473368(A;A)
Alt rs199473368(A;A)
Reference rs199473368(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome not provided
Variation info
Gene KCNJ2
CLNDBN Congenital long QT syndrome not provided
Reversed 0
HGVS NC_000017.10:g.68171380G>A
CLNSRC ClinVar
CLNACC RCV000058295.2, RCV000170972.3,