rs775565634
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs775565634(A;A) |
| Make rs775565634(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 18 |
| Position | 53339808 |
| Gene | DCC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs775565634 |
| dbSNP (classic) | rs775565634 |
| ClinGen | rs775565634 |
| ebi | rs775565634 |
| HLI | rs775565634 |
| Exac | rs775565634 |
| Gnomad | rs775565634 |
| Varsome | rs775565634 |
| LitVar | rs775565634 |
| Map | rs775565634 |
| PheGenI | rs775565634 |
| Biobank | rs775565634 |
| 1000 genomes | rs775565634 |
| hgdp | rs775565634 |
| ensembl | rs775565634 |
| geneview | rs775565634 |
| scholar | rs775565634 |
| rs775565634 | |
| pharmgkb | rs775565634 |
| gwascentral | rs775565634 |
| openSNP | rs775565634 |
| 23andMe | rs775565634 |
| SNPshot | rs775565634 |
| SNPdbe | rs775565634 |
| MSV3d | rs775565634 |
| GWAS Ctlg | rs775565634 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs775565634(A;A) |
| Alt | rs775565634(A;A) |
| Reference | Rs775565634(G;G) |
| Significance | Pathogenic |
| Disease | Corpus callosum agenesis |
| Variation | info |
| Gene | DCC |
| CLNDBN | Corpus callosum agenesis |
| Reversed | 0 |
| HGVS | NC_000018.9:g.50866178G>A |
| CLNSRC | |
| CLNACC | RCV000416318.1, |
