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rs74424227

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs74424227(A;G)
Make rs74424227(G;G)
ReferenceGRCh38 38.1/142
Chromosome21
Position34370759
GeneKCNE2
is asnp
is mentioned by
dbSNPrs74424227
ebirs74424227
HLIrs74424227
Exacrs74424227
Varsomers74424227
Maprs74424227
PheGenIrs74424227
hapmaprs74424227
1000 genomesrs74424227
hgdprs74424227
ensemblrs74424227
gopubmedrs74424227
geneviewrs74424227
scholarrs74424227
googlers74424227
pharmgkbrs74424227
gwascentralrs74424227
openSNPrs74424227
23andMers74424227
23andMe allrs74424227
SNP Nexus

SNPshotrs74424227
SNPdbers74424227
MSV3drs74424227
GWAS Ctlgrs74424227
Max Magnitude0
ClinVar
Risk rs74424227(G;G)
Alt rs74424227(G;G)
Reference rs74424227(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNE2
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000021.8:g.35743058A>G
CLNSRC ClinVar
CLNACC RCV000058372.2,