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rs3764021

From SNPedia

Orientationminus
Stabilizedminus
Make rs3764021(A;A)
Make rs3764021(A;G)
Make rs3764021(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position9681032
GeneCLEC2D
is asnp
is mentioned by
dbSNPrs3764021
ebirs3764021
HLIrs3764021
Exacrs3764021
Varsomers3764021
Maprs3764021
PheGenIrs3764021
hapmaprs3764021
1000 genomesrs3764021
hgdprs3764021
ensemblrs3764021
gopubmedrs3764021
geneviewrs3764021
scholarrs3764021
googlers3764021
pharmgkbrs3764021
gwascentralrs3764021
openSNPrs3764021
23andMers3764021
23andMe allrs3764021
SNP Nexus

SNPshotrs3764021
SNPdbers3764021
MSV3drs3764021
GWAS Ctlgrs3764021
GMAF0.4683
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 17554300OA-icon.png]
Trait Type 1 diabetes
Title Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
Risk Allele C
P-val 4.9999999999999998E-8
Odds Ratio 1.57 [1.38-1.79]


[PMID 17554260OA-icon.png] Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.

[PMID 18462017OA-icon.png] Mapping the genetic architecture of gene expression in human liver.


GET Evidence
rs3764021
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.494513
summary



[PMID 23406209] Association of ZAP70 and PTPN6, but Not BANK1 or CLEC2D, with inflammatory bowel disease in the Tunisian population.