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rs1064793146

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome7
Position150951574
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1064793146
dbSNP (old)rs1064793146
ClinGenrs1064793146
ebirs1064793146
HLIrs1064793146
Exacrs1064793146
Gnomadrs1064793146
Varsomers1064793146
LitVarrs1064793146
Maprs1064793146
PheGenIrs1064793146
Biobankrs1064793146
1000 genomesrs1064793146
hgdprs1064793146
ensemblrs1064793146
gopubmedrs1064793146
geneviewrs1064793146
scholarrs1064793146
googlers1064793146
pharmgkbrs1064793146
gwascentralrs1064793146
openSNPrs1064793146
23andMers1064793146
23andMe allrs1064793146
SNPshotrs1064793146
SNPdbers1064793146
MSV3drs1064793146
GWAS Ctlgrs1064793146
Max Magnitude0
ClinVar
Risk rs1064793146(T;T)
Alt rs1064793146(T;T)
Reference Rs1064793146(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648662T>A
CLNSRC
CLNACC RCV000487402.1,