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rs2287939

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
(T;T) 0 common in clinvar
Make rs2287939(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position33998778
GeneAMACR, C1QTNF3-AMACR
is asnp
is mentioned by
dbSNPrs2287939
dbSNP (classic)rs2287939
ClinGenrs2287939
ebirs2287939
HLIrs2287939
Exacrs2287939
Gnomadrs2287939
Varsomers2287939
LitVarrs2287939
Maprs2287939
PheGenIrs2287939
Biobankrs2287939
1000 genomesrs2287939
hgdprs2287939
ensemblrs2287939
geneviewrs2287939
scholarrs2287939
googlers2287939
pharmgkbrs2287939
gwascentralrs2287939
openSNPrs2287939
23andMers2287939
SNPshotrs2287939
SNPdbers2287939
MSV3drs2287939
GWAS Ctlgrs2287939
GMAF0.2374
Max Magnitude0
? (C;C) (C;T) (T;T) 28




[PMID 20945498OA-icon.png] AMACR polymorphisms, dietary intake of red meat and dairy and prostate cancer risk

[PMID 20445798OA-icon.png] Chromosome 5p Region SNPs Are Associated with Risk of NSCLC among Women.

[PMID 20875727OA-icon.png] Non-synonymous variants in the AMACR gene are associated with schizophrenia.



ClinVar
Risk Rs2287939(C;C) rs2287939(G;G)
Alt Rs2287939(C;C) rs2287939(G;G)
Reference Rs2287939(T;T)
Significance Other
Disease not specified Alpha-methylacyl-CoA racemase deficiency
Variation info
Gene C1QTNF3-AMACR AMACR
CLNDBN not specified Alpha-methylacyl-CoA racemase deficiency
Reversed 1
HGVS NC_000005.9:g.33998883A>G
CLNSRC UniProtKB (protein)
CLNACC RCV000116322.3, RCV000276161.1,