rs3916765
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common on affy axiom data |
| Make rs3916765(A;A) |
| Make rs3916765(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32717773 |
| Gene | LOC102725019 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3916765 |
| dbSNP (classic) | rs3916765 |
| ClinGen | rs3916765 |
| ebi | rs3916765 |
| HLI | rs3916765 |
| Exac | rs3916765 |
| Gnomad | rs3916765 |
| Varsome | rs3916765 |
| LitVar | rs3916765 |
| Map | rs3916765 |
| PheGenI | rs3916765 |
| Biobank | rs3916765 |
| 1000 genomes | rs3916765 |
| hgdp | rs3916765 |
| ensembl | rs3916765 |
| geneview | rs3916765 |
| scholar | rs3916765 |
| rs3916765 | |
| pharmgkb | rs3916765 |
| gwascentral | rs3916765 |
| openSNP | rs3916765 |
| 23andMe | rs3916765 |
| SNPshot | rs3916765 |
| SNPdbe | rs3916765 |
| MSV3d | rs3916765 |
| GWAS Ctlg | rs3916765 |
| GMAF | 0.09871 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22693455 ]
|
| Trait | |
| Title | Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases. |
| Risk Allele | A |
| P-val | 0.000001 |
| Odds Ratio | 1.2100 None |
[PMID 19143815] MHC fine mapping of human type 1 diabetes using the T1DGC data.
[PMID 19143817] Effect of linkage status of affected sib-pairs on the search for novel type 1 diabetes susceptibility genes in the HLA complex.
