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rs1064794779

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome12
Position21828990
GeneABCC9, LOC105369689
is asnp
is mentioned by
dbSNPrs1064794779
dbSNP (old)rs1064794779
ClinGenrs1064794779
ebirs1064794779
HLIrs1064794779
Exacrs1064794779
Gnomadrs1064794779
Varsomers1064794779
LitVarrs1064794779
Maprs1064794779
PheGenIrs1064794779
Biobankrs1064794779
1000 genomesrs1064794779
hgdprs1064794779
ensemblrs1064794779
gopubmedrs1064794779
geneviewrs1064794779
scholarrs1064794779
googlers1064794779
pharmgkbrs1064794779
gwascentralrs1064794779
openSNPrs1064794779
23andMers1064794779
23andMe allrs1064794779
SNPshotrs1064794779
SNPdbers1064794779
MSV3drs1064794779
GWAS Ctlgrs1064794779
Max Magnitude0
ClinVar
Risk rs1064794779(G;G)
Alt rs1064794779(G;G)
Reference Rs1064794779(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCC9
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.21981924A>C
CLNSRC
CLNACC RCV000487267.1,