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rs199473367

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473367(C;T)
Make rs199473367(T;T)
ReferenceGRCh38 38.1/142
Chromosome21
Position34370825
GeneKCNE2
is asnp
is mentioned by
dbSNPrs199473367
ebirs199473367
HLIrs199473367
Exacrs199473367
Varsomers199473367
Maprs199473367
PheGenIrs199473367
hapmaprs199473367
1000 genomesrs199473367
hgdprs199473367
ensemblrs199473367
gopubmedrs199473367
geneviewrs199473367
scholarrs199473367
googlers199473367
pharmgkbrs199473367
gwascentralrs199473367
openSNPrs199473367
23andMers199473367
23andMe allrs199473367
SNP Nexus

SNPshotrs199473367
SNPdbers199473367
MSV3drs199473367
GWAS Ctlgrs199473367
Max Magnitude0
ClinVar
Risk rs199473367(T;T)
Alt rs199473367(T;T)
Reference rs199473367(C;C)
Significance Pathogenic
Disease Acquired long QT syndrome not provided
Variation info
Gene KCNE2
CLNDBN Acquired long QT syndrome not provided
Reversed 0
HGVS NC_000021.8:g.35743124C>T
CLNSRC ClinVar
CLNACC RCV000058374.2, RCV000222131.1,