rs269949
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs269949(A;A) |
| Make rs269949(A;G) |
| Make rs269949(G;G) |
| Reference | GRCh37.p5 37.3/137 |
| Chromosome | 19 |
| Position | 54930401 |
| Gene | NCR1, NLRP7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs269949 |
| dbSNP (classic) | rs269949 |
| ClinGen | rs269949 |
| ebi | rs269949 |
| HLI | rs269949 |
| Exac | rs269949 |
| Gnomad | rs269949 |
| Varsome | rs269949 |
| LitVar | rs269949 |
| Map | rs269949 |
| PheGenI | rs269949 |
| Biobank | rs269949 |
| 1000 genomes | rs269949 |
| hgdp | rs269949 |
| ensembl | rs269949 |
| geneview | rs269949 |
| scholar | rs269949 |
| rs269949 | |
| pharmgkb | rs269949 |
| gwascentral | rs269949 |
| openSNP | rs269949 |
| 23andMe | rs269949 |
| SNPshot | rs269949 |
| SNPdbe | rs269949 |
| MSV3d | rs269949 |
| GWAS Ctlg | rs269949 |
| GMAF | 0.4252 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23360675] A genetic association study of NLRP2 and NLRP7 genes in idiopathic recurrent miscarriage
