rs201849460
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs201849460(A;A) |
| Make rs201849460(A;G) |
| Make rs201849460(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 3 |
| Position | 186620776 |
| Gene | AHSG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs201849460 |
| dbSNP (classic) | rs201849460 |
| ClinGen | rs201849460 |
| ebi | rs201849460 |
| HLI | rs201849460 |
| Exac | rs201849460 |
| Gnomad | rs201849460 |
| Varsome | rs201849460 |
| LitVar | rs201849460 |
| Map | rs201849460 |
| PheGenI | rs201849460 |
| Biobank | rs201849460 |
| 1000 genomes | rs201849460 |
| hgdp | rs201849460 |
| ensembl | rs201849460 |
| geneview | rs201849460 |
| scholar | rs201849460 |
| rs201849460 | |
| pharmgkb | rs201849460 |
| gwascentral | rs201849460 |
| openSNP | rs201849460 |
| 23andMe | rs201849460 |
| SNPshot | rs201849460 |
| SNPdbe | rs201849460 |
| MSV3d | rs201849460 |
| GWAS Ctlg | rs201849460 |
| Max Magnitude | 0 |
OMIM pathogenic variant
