rs10174098
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10174098(A;A) |
| Make rs10174098(A;G) |
| Make rs10174098(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 186628015 |
| Gene | ITGAV |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10174098 |
| dbSNP (classic) | rs10174098 |
| ClinGen | rs10174098 |
| ebi | rs10174098 |
| HLI | rs10174098 |
| Exac | rs10174098 |
| Gnomad | rs10174098 |
| Varsome | rs10174098 |
| LitVar | rs10174098 |
| Map | rs10174098 |
| PheGenI | rs10174098 |
| Biobank | rs10174098 |
| 1000 genomes | rs10174098 |
| hgdp | rs10174098 |
| ensembl | rs10174098 |
| geneview | rs10174098 |
| scholar | rs10174098 |
| rs10174098 | |
| pharmgkb | rs10174098 |
| gwascentral | rs10174098 |
| openSNP | rs10174098 |
| 23andMe | rs10174098 |
| SNPshot | rs10174098 |
| SNPdbe | rs10174098 |
| MSV3d | rs10174098 |
| GWAS Ctlg | rs10174098 |
| GMAF | 0.3586 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19818132
] The ITGAV rs3738919 variant and susceptibility to rheumatoid arthritis in four Caucasian sample sets
[PMID 21116829] A polymorphism in the integrin alphaV subunit gene affects the progression of primary biliary cirrhosis in Japanese patients.
