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rs199473386

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473386(A;A)
Make rs199473386(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175946
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473386
ebirs199473386
HLIrs199473386
Exacrs199473386
Varsomers199473386
Maprs199473386
PheGenIrs199473386
hapmaprs199473386
1000 genomesrs199473386
hgdprs199473386
ensemblrs199473386
gopubmedrs199473386
geneviewrs199473386
scholarrs199473386
googlers199473386
pharmgkbrs199473386
gwascentralrs199473386
openSNPrs199473386
23andMers199473386
23andMe allrs199473386
SNP Nexus

SNPshotrs199473386
SNPdbers199473386
MSV3drs199473386
GWAS Ctlgrs199473386
Max Magnitude0
ClinVar
Risk rs199473386(A;A)
Alt rs199473386(A;A)
Reference rs199473386(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.68172087G>A
CLNSRC ClinVar
CLNACC RCV000058334.2,