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

rs199473376

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473376(C;T)
Make rs199473376(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175446
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473376
ebirs199473376
HLIrs199473376
Exacrs199473376
Varsomers199473376
Maprs199473376
PheGenIrs199473376
hapmaprs199473376
1000 genomesrs199473376
hgdprs199473376
ensemblrs199473376
gopubmedrs199473376
geneviewrs199473376
scholarrs199473376
googlers199473376
pharmgkbrs199473376
gwascentralrs199473376
openSNPrs199473376
23andMers199473376
23andMe allrs199473376
SNP Nexus

SNPshotrs199473376
SNPdbers199473376
MSV3drs199473376
GWAS Ctlgrs199473376
Max Magnitude0
ClinVar
Risk rs199473376(T;T)
Alt rs199473376(T;T)
Reference rs199473376(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.68171587C>T
CLNSRC ClinVar
CLNACC RCV000058310.2,