rs199469494
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs199469494(A;A) |
| Make rs199469494(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 93892928 |
| Gene | PROS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs199469494 |
| dbSNP (classic) | rs199469494 |
| ClinGen | rs199469494 |
| ebi | rs199469494 |
| HLI | rs199469494 |
| Exac | rs199469494 |
| Gnomad | rs199469494 |
| Varsome | rs199469494 |
| LitVar | rs199469494 |
| Map | rs199469494 |
| PheGenI | rs199469494 |
| Biobank | rs199469494 |
| 1000 genomes | rs199469494 |
| hgdp | rs199469494 |
| ensembl | rs199469494 |
| geneview | rs199469494 |
| scholar | rs199469494 |
| rs199469494 | |
| pharmgkb | rs199469494 |
| gwascentral | rs199469494 |
| openSNP | rs199469494 |
| 23andMe | rs199469494 |
| SNPshot | rs199469494 |
| SNPdbe | rs199469494 |
| MSV3d | rs199469494 |
| GWAS Ctlg | rs199469494 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs199469494(A;A) |
| Alt | rs199469494(A;A) |
| Reference | Rs199469494(G;G) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | PROS1 |
| CLNDBN | OMIM |
| Reversed | 1 |
| HGVS | NC_000003.11:g.93611772C>T |
| CLNSRC | |
| CLNACC | |
