Have questions? Visit https://www.reddit.com/r/SNPedia

rs199473388

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473388(C;T)
Make rs199473388(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175965
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473388
ebirs199473388
HLIrs199473388
Exacrs199473388
Varsomers199473388
Maprs199473388
PheGenIrs199473388
hapmaprs199473388
1000 genomesrs199473388
hgdprs199473388
ensemblrs199473388
gopubmedrs199473388
geneviewrs199473388
scholarrs199473388
googlers199473388
pharmgkbrs199473388
gwascentralrs199473388
openSNPrs199473388
23andMers199473388
23andMe allrs199473388
SNP Nexus

SNPshotrs199473388
SNPdbers199473388
MSV3drs199473388
GWAS Ctlgrs199473388
Max Magnitude0
ClinVar
Risk rs199473388(T;T)
Alt rs199473388(T;T)
Reference rs199473388(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.68172106C>T
CLNSRC ClinVar
CLNACC RCV000058338.2,