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rs1064794780

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome12
Position21828971
GeneABCC9, LOC105369689
is asnp
is mentioned by
dbSNPrs1064794780
dbSNP (old)rs1064794780
ClinGenrs1064794780
ebirs1064794780
HLIrs1064794780
Exacrs1064794780
Gnomadrs1064794780
Varsomers1064794780
Maprs1064794780
PheGenIrs1064794780
Biobankrs1064794780
1000 genomesrs1064794780
hgdprs1064794780
ensemblrs1064794780
gopubmedrs1064794780
geneviewrs1064794780
scholarrs1064794780
googlers1064794780
pharmgkbrs1064794780
gwascentralrs1064794780
openSNPrs1064794780
23andMers1064794780
23andMe allrs1064794780
SNPshotrs1064794780
SNPdbers1064794780
MSV3drs1064794780
GWAS Ctlgrs1064794780
Max Magnitude0
ClinVar
Risk rs1064794780(G;G)
Alt rs1064794780(G;G)
Reference Rs1064794780(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCC9
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.21981905A>C
CLNSRC
CLNACC RCV000480387.1,