rs45450798
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs45450798(C;C) |
Make rs45450798(C;G) |
Make rs45450798(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 12792941 |
Gene | PTPN2 |
is a | snp |
is | mentioned by |
dbSNP | rs45450798 |
dbSNP (classic) | rs45450798 |
ClinGen | rs45450798 |
ebi | rs45450798 |
HLI | rs45450798 |
Exac | rs45450798 |
Gnomad | rs45450798 |
Varsome | rs45450798 |
LitVar | rs45450798 |
Map | rs45450798 |
PheGenI | rs45450798 |
Biobank | rs45450798 |
1000 genomes | rs45450798 |
hgdp | rs45450798 |
ensembl | rs45450798 |
geneview | rs45450798 |
scholar | rs45450798 |
rs45450798 | |
pharmgkb | rs45450798 |
gwascentral | rs45450798 |
openSNP | rs45450798 |
23andMe | rs45450798 |
SNPshot | rs45450798 |
SNPdbe | rs45450798 |
MSV3d | rs45450798 |
GWAS Ctlg | rs45450798 |
GMAF | 0.1194 |
Max Magnitude | 0 |
[PMID 19073967] Shared and distinct genetic variants in type 1 diabetes and celiac disease.
[PMID 26074154] Non-HLA gene effects on the disease process of type 1 diabetes: From HLA susceptibility to overt disease.