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rs1001916923

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1001916923(A;G)
Make rs1001916923(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position21908147
GeneABCC9
is asnp
is mentioned by
dbSNPrs1001916923
dbSNP (old)rs1001916923
ClinGenrs1001916923
ebirs1001916923
HLIrs1001916923
Exacrs1001916923
Gnomadrs1001916923
Varsomers1001916923
Maprs1001916923
PheGenIrs1001916923
Biobankrs1001916923
1000 genomesrs1001916923
hgdprs1001916923
ensemblrs1001916923
gopubmedrs1001916923
geneviewrs1001916923
scholarrs1001916923
googlers1001916923
pharmgkbrs1001916923
gwascentralrs1001916923
openSNPrs1001916923
23andMers1001916923
23andMe allrs1001916923
SNP Nexus

SNPshotrs1001916923
SNPdbers1001916923
MSV3drs1001916923
GWAS Ctlgrs1001916923
Max Magnitude0
ClinVar
Risk rs1001916923(G;G) rs1001916923(T;T)
Alt rs1001916923(G;G) rs1001916923(T;T)
Reference Rs1001916923(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.22061081A>G
CLNSRC
CLNACC RCV000486887.1,