rs199881207
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs199881207(A;A) |
| Make rs199881207(A;G) |
| Make rs199881207(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 19 |
| Position | 53810605 |
| Gene | NLRP12 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs199881207 |
| dbSNP (classic) | rs199881207 |
| ClinGen | rs199881207 |
| ebi | rs199881207 |
| HLI | rs199881207 |
| Exac | rs199881207 |
| Gnomad | rs199881207 |
| Varsome | rs199881207 |
| LitVar | rs199881207 |
| Map | rs199881207 |
| PheGenI | rs199881207 |
| Biobank | rs199881207 |
| 1000 genomes | rs199881207 |
| hgdp | rs199881207 |
| ensembl | rs199881207 |
| geneview | rs199881207 |
| scholar | rs199881207 |
| rs199881207 | |
| pharmgkb | rs199881207 |
| gwascentral | rs199881207 |
| openSNP | rs199881207 |
| 23andMe | rs199881207 |
| SNPshot | rs199881207 |
| SNPdbe | rs199881207 |
| MSV3d | rs199881207 |
| GWAS Ctlg | rs199881207 |
| Max Magnitude | 0 |
OMIM pathogenic variant
