rs3911238
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3911238(C;C) |
| Make rs3911238(C;G) |
| Make rs3911238(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 186605617 |
| Gene | ITGAV |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3911238 |
| dbSNP (classic) | rs3911238 |
| ClinGen | rs3911238 |
| ebi | rs3911238 |
| HLI | rs3911238 |
| Exac | rs3911238 |
| Gnomad | rs3911238 |
| Varsome | rs3911238 |
| LitVar | rs3911238 |
| Map | rs3911238 |
| PheGenI | rs3911238 |
| Biobank | rs3911238 |
| 1000 genomes | rs3911238 |
| hgdp | rs3911238 |
| ensembl | rs3911238 |
| geneview | rs3911238 |
| scholar | rs3911238 |
| rs3911238 | |
| pharmgkb | rs3911238 |
| gwascentral | rs3911238 |
| openSNP | rs3911238 |
| 23andMe | rs3911238 |
| SNPshot | rs3911238 |
| SNPdbe | rs3911238 |
| MSV3d | rs3911238 |
| GWAS Ctlg | rs3911238 |
| GMAF | 0.3522 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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.
