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rs751931568

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs751931568(A;A)
Make rs751931568(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome21
Position34370687
GeneKCNE2, LOC105372791
is asnp
is mentioned by
dbSNPrs751931568
ebirs751931568
HLIrs751931568
Exacrs751931568
Varsomers751931568
Maprs751931568
PheGenIrs751931568
hapmaprs751931568
1000 genomesrs751931568
hgdprs751931568
ensemblrs751931568
gopubmedrs751931568
geneviewrs751931568
scholarrs751931568
googlers751931568
pharmgkbrs751931568
gwascentralrs751931568
openSNPrs751931568
23andMers751931568
23andMe allrs751931568
SNP Nexus

SNPshotrs751931568
SNPdbers751931568
MSV3drs751931568
GWAS Ctlgrs751931568
Max Magnitude0
ClinVar
Risk rs751931568(A;A)
Alt rs751931568(A;A)
Reference rs751931568(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNE2
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.35742986G>A
CLNSRC
CLNACC RCV000171348.1,