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rs9976767

From SNPedia

Orientationplus
Stabilizedplus
Make rs9976767(A;A)
Make rs9976767(A;G)
Make rs9976767(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position42416281
GeneUBASH3A
is asnp
is mentioned by
dbSNPrs9976767
ebirs9976767
HLIrs9976767
Exacrs9976767
Varsomers9976767
Maprs9976767
PheGenIrs9976767
hapmaprs9976767
1000 genomesrs9976767
hgdprs9976767
ensemblrs9976767
gopubmedrs9976767
geneviewrs9976767
scholarrs9976767
googlers9976767
pharmgkbrs9976767
gwascentralrs9976767
openSNPrs9976767
23andMers9976767
23andMe allrs9976767
SNP Nexus

SNPshotrs9976767
SNPdbers9976767
MSV3drs9976767
GWAS Ctlgrs9976767
GMAF0.4201
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18840781OA-icon.png]
Trait Type 1 diabetes
Title Follow up analysis of genome-wide association data identifies novel loci for type 1 diabetes
Risk Allele C
P-val 2E-8
Odds Ratio 1.16 [1.10-1.22]




GET Evidence
rs9976767
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.476562
summary