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rs144022753

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs144022753(C;T)
Make rs144022753(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position70176238
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs144022753
ebirs144022753
HLIrs144022753
Exacrs144022753
Varsomers144022753
Maprs144022753
PheGenIrs144022753
hapmaprs144022753
1000 genomesrs144022753
hgdprs144022753
ensemblrs144022753
gopubmedrs144022753
geneviewrs144022753
scholarrs144022753
googlers144022753
pharmgkbrs144022753
gwascentralrs144022753
openSNPrs144022753
23andMers144022753
23andMe allrs144022753
SNP Nexus

SNPshotrs144022753
SNPdbers144022753
MSV3drs144022753
GWAS Ctlgrs144022753
Max Magnitude0
ClinVar
Risk rs144022753(G,T;G,T)
Alt rs144022753(G,T;G,T)
Reference rs144022753(C;C)
Significance Probable-Pathogenic
Disease Long QT syndrome not provided
Variation info
Gene KCNJ2
CLNDBN Long QT syndrome not provided
Reversed 0
HGVS NC_000017.10:g.68172379C>T
CLNSRC
CLNACC RCV000148542.1, RCV000170991.3,