rs10999426
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10999426(A;A) |
| Make rs10999426(A;G) |
| Make rs10999426(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 70600282 |
| Gene | PRF1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10999426 |
| dbSNP (classic) | rs10999426 |
| ClinGen | rs10999426 |
| ebi | rs10999426 |
| HLI | rs10999426 |
| Exac | rs10999426 |
| Gnomad | rs10999426 |
| Varsome | rs10999426 |
| LitVar | rs10999426 |
| Map | rs10999426 |
| PheGenI | rs10999426 |
| Biobank | rs10999426 |
| 1000 genomes | rs10999426 |
| hgdp | rs10999426 |
| ensembl | rs10999426 |
| geneview | rs10999426 |
| scholar | rs10999426 |
| rs10999426 | |
| pharmgkb | rs10999426 |
| gwascentral | rs10999426 |
| openSNP | rs10999426 |
| 23andMe | rs10999426 |
| SNPshot | rs10999426 |
| SNPdbe | rs10999426 |
| MSV3d | rs10999426 |
| GWAS Ctlg | rs10999426 |
| GMAF | 0.1662 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20921521] Gender-associated differences of perforin polymorphisms in the susceptibility to multiple sclerosis
[PMID 16385451
] A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.
[PMID 23528102] Association between granzyme B and perforin I polymorphisms and allograft outcomes in Hispanic kidney transplant recipients
