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rs199473378

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473378(A;A)
Make rs199473378(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175469
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473378
ebirs199473378
HLIrs199473378
Exacrs199473378
Varsomers199473378
Maprs199473378
PheGenIrs199473378
hapmaprs199473378
1000 genomesrs199473378
hgdprs199473378
ensemblrs199473378
gopubmedrs199473378
geneviewrs199473378
scholarrs199473378
googlers199473378
pharmgkbrs199473378
gwascentralrs199473378
openSNPrs199473378
23andMers199473378
23andMe allrs199473378
SNP Nexus

SNPshotrs199473378
SNPdbers199473378
MSV3drs199473378
GWAS Ctlgrs199473378
Max Magnitude0
ClinVar
Risk rs199473378(A;A)
Alt rs199473378(A;A)
Reference rs199473378(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.68171610G>A
CLNSRC ClinVar
CLNACC RCV000058311.2,