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rs786205807

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205807(A;A)
Make rs786205807(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome21
Position34370840
GeneKCNE2, LOC105372791
is asnp
is mentioned by
dbSNPrs786205807
ebirs786205807
HLIrs786205807
Exacrs786205807
Varsomers786205807
Maprs786205807
PheGenIrs786205807
hapmaprs786205807
1000 genomesrs786205807
hgdprs786205807
ensemblrs786205807
gopubmedrs786205807
geneviewrs786205807
scholarrs786205807
googlers786205807
pharmgkbrs786205807
gwascentralrs786205807
openSNPrs786205807
23andMers786205807
23andMe allrs786205807
SNP Nexus

SNPshotrs786205807
SNPdbers786205807
MSV3drs786205807
GWAS Ctlgrs786205807
Max Magnitude0
ClinVar
Risk rs786205807(A;A)
Alt rs786205807(A;A)
Reference rs786205807(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNE2
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.35743139T>A
CLNSRC
CLNACC RCV000170958.3,