rs77888940
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs77888940(C;G) |
| Make rs77888940(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 6 |
| Position | 1610017 |
| Gene | FOXC1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs77888940 |
| dbSNP (classic) | rs77888940 |
| ClinGen | rs77888940 |
| ebi | rs77888940 |
| HLI | rs77888940 |
| Exac | rs77888940 |
| Gnomad | rs77888940 |
| Varsome | rs77888940 |
| LitVar | rs77888940 |
| Map | rs77888940 |
| PheGenI | rs77888940 |
| Biobank | rs77888940 |
| 1000 genomes | rs77888940 |
| hgdp | rs77888940 |
| ensembl | rs77888940 |
| geneview | rs77888940 |
| scholar | rs77888940 |
| rs77888940 | |
| pharmgkb | rs77888940 |
| gwascentral | rs77888940 |
| openSNP | rs77888940 |
| 23andMe | rs77888940 |
| SNPshot | rs77888940 |
| SNPdbe | rs77888940 |
| MSV3d | rs77888940 |
| GWAS Ctlg | rs77888940 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs77888940(G;G) |
| Alt | rs77888940(G;G) |
| Reference | Rs77888940(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | FOXC1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000006.11:g.1610252C>G |
| CLNSRC | |
| CLNACC | RCV000162084.1, |
