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rs1064794793

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome7
Position150950983
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1064794793
dbSNP (classic)rs1064794793
ClinGenrs1064794793
ebirs1064794793
HLIrs1064794793
Exacrs1064794793
Gnomadrs1064794793
Varsomers1064794793
LitVarrs1064794793
Maprs1064794793
PheGenIrs1064794793
Biobankrs1064794793
1000 genomesrs1064794793
hgdprs1064794793
ensemblrs1064794793
geneviewrs1064794793
scholarrs1064794793
googlers1064794793
pharmgkbrs1064794793
gwascentralrs1064794793
openSNPrs1064794793
23andMers1064794793
23andMe allrs1064794793
SNPshotrs1064794793
SNPdbers1064794793
MSV3drs1064794793
GWAS Ctlgrs1064794793
Max Magnitude0
ClinVar
Risk rs1064794793(T;T)
Alt rs1064794793(T;T)
Reference Rs1064794793(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648071G>A
CLNSRC
CLNACC RCV000481174.1,