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rs1064794494

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Chromosome7
Position150955470
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1064794494
dbSNP (old)rs1064794494
ClinGenrs1064794494
ebirs1064794494
HLIrs1064794494
Exacrs1064794494
Gnomadrs1064794494
Varsomers1064794494
Maprs1064794494
PheGenIrs1064794494
Biobankrs1064794494
1000 genomesrs1064794494
hgdprs1064794494
ensemblrs1064794494
gopubmedrs1064794494
geneviewrs1064794494
scholarrs1064794494
googlers1064794494
pharmgkbrs1064794494
gwascentralrs1064794494
openSNPrs1064794494
23andMers1064794494
23andMe allrs1064794494
SNPshotrs1064794494
SNPdbers1064794494
MSV3drs1064794494
GWAS Ctlgrs1064794494
Max Magnitude0
ClinVar
Risk rs1064794494(-;-)
Alt rs1064794494(-;-)
Reference Rs1064794494(AG;AG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150652558_150652559delCT
CLNSRC
CLNACC RCV000483726.1,