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rs199473382

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473382(A;G)
Make rs199473382(G;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175613
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473382
ebirs199473382
HLIrs199473382
Exacrs199473382
Varsomers199473382
Maprs199473382
PheGenIrs199473382
hapmaprs199473382
1000 genomesrs199473382
hgdprs199473382
ensemblrs199473382
gopubmedrs199473382
geneviewrs199473382
scholarrs199473382
googlers199473382
pharmgkbrs199473382
gwascentralrs199473382
openSNPrs199473382
23andMers199473382
23andMe allrs199473382
SNP Nexus

SNPshotrs199473382
SNPdbers199473382
MSV3drs199473382
GWAS Ctlgrs199473382
Max Magnitude0
ClinVar
Risk rs199473382(G;G)
Alt rs199473382(G;G)
Reference rs199473382(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.68171754A>G
CLNSRC ClinVar
CLNACC RCV000058321.2,