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rs1064793147

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome7
Position150948980
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1064793147
dbSNP (old)rs1064793147
ClinGenrs1064793147
ebirs1064793147
HLIrs1064793147
Exacrs1064793147
Gnomadrs1064793147
Varsomers1064793147
Maprs1064793147
PheGenIrs1064793147
Biobankrs1064793147
1000 genomesrs1064793147
hgdprs1064793147
ensemblrs1064793147
gopubmedrs1064793147
geneviewrs1064793147
scholarrs1064793147
googlers1064793147
pharmgkbrs1064793147
gwascentralrs1064793147
openSNPrs1064793147
23andMers1064793147
23andMe allrs1064793147
SNPshotrs1064793147
SNPdbers1064793147
MSV3drs1064793147
GWAS Ctlgrs1064793147
Max Magnitude0
ClinVar
Risk rs1064793147(A;A)
Alt rs1064793147(A;A)
Reference Rs1064793147(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150646068C>T
CLNSRC
CLNACC RCV000481087.1,