rs766325
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs766325(A;A) |
| Make rs766325(A;G) |
| Make rs766325(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 18629964 |
| Gene | PAX7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs766325 |
| dbSNP (classic) | rs766325 |
| ClinGen | rs766325 |
| ebi | rs766325 |
| HLI | rs766325 |
| Exac | rs766325 |
| Gnomad | rs766325 |
| Varsome | rs766325 |
| LitVar | rs766325 |
| Map | rs766325 |
| PheGenI | rs766325 |
| Biobank | rs766325 |
| 1000 genomes | rs766325 |
| hgdp | rs766325 |
| ensembl | rs766325 |
| geneview | rs766325 |
| scholar | rs766325 |
| rs766325 | |
| pharmgkb | rs766325 |
| gwascentral | rs766325 |
| openSNP | rs766325 |
| 23andMe | rs766325 |
| SNPshot | rs766325 |
| SNPdbe | rs766325 |
| MSV3d | rs766325 |
| GWAS Ctlg | rs766325 |
| GMAF | 0.4954 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19142206
] Maternal transmission effects of the PAX genes among cleft case-parent trios from four populations
[PMID 23463464] Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P).
