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rs199473659

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473659(C;T)
Make rs199473659(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position70176090
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473659
ebirs199473659
HLIrs199473659
Exacrs199473659
Varsomers199473659
Maprs199473659
PheGenIrs199473659
hapmaprs199473659
1000 genomesrs199473659
hgdprs199473659
ensemblrs199473659
gopubmedrs199473659
geneviewrs199473659
scholarrs199473659
googlers199473659
pharmgkbrs199473659
gwascentralrs199473659
openSNPrs199473659
23andMers199473659
23andMe allrs199473659
SNP Nexus

SNPshotrs199473659
SNPdbers199473659
MSV3drs199473659
GWAS Ctlgrs199473659
Max Magnitude0
ClinVar
Risk rs199473659(T;T)
Alt rs199473659(T;T)
Reference rs199473659(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNJ2
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000017.10:g.68172231C>T
CLNSRC ClinVar
CLNACC RCV000058291.2,