rs774895361
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs774895361(A;A) |
| Make rs774895361(A;C) |
| Make rs774895361(C;C) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 19 |
| Position | 53810436 |
| Gene | NLRP12 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs774895361 |
| dbSNP (classic) | rs774895361 |
| ClinGen | rs774895361 |
| ebi | rs774895361 |
| HLI | rs774895361 |
| Exac | rs774895361 |
| Gnomad | rs774895361 |
| Varsome | rs774895361 |
| LitVar | rs774895361 |
| Map | rs774895361 |
| PheGenI | rs774895361 |
| Biobank | rs774895361 |
| 1000 genomes | rs774895361 |
| hgdp | rs774895361 |
| ensembl | rs774895361 |
| geneview | rs774895361 |
| scholar | rs774895361 |
| rs774895361 | |
| pharmgkb | rs774895361 |
| gwascentral | rs774895361 |
| openSNP | rs774895361 |
| 23andMe | rs774895361 |
| SNPshot | rs774895361 |
| SNPdbe | rs774895361 |
| MSV3d | rs774895361 |
| GWAS Ctlg | rs774895361 |
| Max Magnitude | 0 |
aka NM_001277126.1(NLRP12):c.1223G>A or (p.Trp408Ter)
OMIM pathogenic variant
