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rs786205806

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205806(A;A)
Make rs786205806(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome21
Position34364156
GeneKCNE2, LOC105372791
is asnp
is mentioned by
dbSNPrs786205806
dbSNP (old)rs786205806
ClinGenrs786205806
ebirs786205806
HLIrs786205806
Exacrs786205806
Gnomadrs786205806
Varsomers786205806
Maprs786205806
PheGenIrs786205806
Biobankrs786205806
1000 genomesrs786205806
hgdprs786205806
ensemblrs786205806
gopubmedrs786205806
geneviewrs786205806
scholarrs786205806
googlers786205806
pharmgkbrs786205806
gwascentralrs786205806
openSNPrs786205806
23andMers786205806
23andMe allrs786205806
SNP Nexus

SNPshotrs786205806
SNPdbers786205806
MSV3drs786205806
GWAS Ctlgrs786205806
Max Magnitude0
ClinVar
Risk rs786205806(A;A)
Alt rs786205806(A;A)
Reference Rs786205806(G;G)
Significance Probable-Pathogenic
Disease Familial atrial fibrillation Romano-Ward syndrome Long QT syndrome
Variation info
Gene KCNE2
CLNDBN Familial atrial fibrillation Romano-Ward syndrome Long QT syndrome
Reversed 0
HGVS NC_000021.8:g.35736455G>A
CLNSRC
CLNACC RCV000288510.1, RCV000331921.1, RCV000381892.1,