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

rs199473655

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473655(C;T)
Make rs199473655(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175614
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473655
ebirs199473655
HLIrs199473655
Exacrs199473655
Varsomers199473655
Maprs199473655
PheGenIrs199473655
hapmaprs199473655
1000 genomesrs199473655
hgdprs199473655
ensemblrs199473655
gopubmedrs199473655
geneviewrs199473655
scholarrs199473655
googlers199473655
pharmgkbrs199473655
gwascentralrs199473655
openSNPrs199473655
23andMers199473655
23andMe allrs199473655
SNP Nexus

SNPshotrs199473655
SNPdbers199473655
MSV3drs199473655
GWAS Ctlgrs199473655
Max Magnitude0
ClinVar
Risk rs199473655(T;T)
Alt rs199473655(T;T)
Reference rs199473655(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.68171755C>T
CLNSRC ClinVar
CLNACC RCV000058322.2,