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rs786205588

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205588(C;C)
Make rs786205588(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951655
GeneKCNH2
is asnp
is mentioned by
dbSNPrs786205588
ebirs786205588
HLIrs786205588
Exacrs786205588
Varsomers786205588
Maprs786205588
PheGenIrs786205588
hapmaprs786205588
1000 genomesrs786205588
hgdprs786205588
ensemblrs786205588
gopubmedrs786205588
geneviewrs786205588
scholarrs786205588
googlers786205588
pharmgkbrs786205588
gwascentralrs786205588
openSNPrs786205588
23andMers786205588
23andMe allrs786205588
SNP Nexus

SNPshotrs786205588
SNPdbers786205588
MSV3drs786205588
GWAS Ctlgrs786205588
Max Magnitude0
ClinVar
Risk rs786205588(C;C)
Alt rs786205588(C;C)
Reference rs786205588(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648743C>G
CLNSRC
CLNACC RCV000171410.1,