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rs199473366

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473366(A;G)
Make rs199473366(G;G)
ReferenceGRCh38 38.1/142
Chromosome21
Position34370747
GeneKCNE2, LOC105372791
is asnp
is mentioned by
dbSNPrs199473366
dbSNP (classic)rs199473366
ClinGenrs199473366
ebirs199473366
HLIrs199473366
Exacrs199473366
Gnomadrs199473366
Varsomers199473366
LitVarrs199473366
Maprs199473366
PheGenIrs199473366
Biobankrs199473366
1000 genomesrs199473366
hgdprs199473366
ensemblrs199473366
geneviewrs199473366
scholarrs199473366
googlers199473366
pharmgkbrs199473366
gwascentralrs199473366
openSNPrs199473366
23andMers199473366
SNPshotrs199473366
SNPdbers199473366
MSV3drs199473366
GWAS Ctlgrs199473366
Max Magnitude0
ClinVar
Risk rs199473366(G;G)
Alt rs199473366(G;G)
Reference Rs199473366(A;A)
Significance Untested
Disease Atrial fibrillation
Variation info
Gene KCNE2
CLNDBN Atrial fibrillation
Reversed 0
HGVS NC_000021.8:g.35743046A>G
CLNSRC ClinVar
CLNACC RCV000058371.3,