rs764611160
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (AG;AG) | 0 | common in clinvar |
| Make rs764611160(-;-) |
| Make rs764611160(-;AG) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 7 |
| Position | 107915624 |
| Gene | DLD |
| is a | snp |
| is | mentioned by |
| dbSNP | rs764611160 |
| dbSNP (classic) | rs764611160 |
| ClinGen | rs764611160 |
| ebi | rs764611160 |
| HLI | rs764611160 |
| Exac | rs764611160 |
| Gnomad | rs764611160 |
| Varsome | rs764611160 |
| LitVar | rs764611160 |
| Map | rs764611160 |
| PheGenI | rs764611160 |
| Biobank | rs764611160 |
| 1000 genomes | rs764611160 |
| hgdp | rs764611160 |
| ensembl | rs764611160 |
| geneview | rs764611160 |
| scholar | rs764611160 |
| rs764611160 | |
| pharmgkb | rs764611160 |
| gwascentral | rs764611160 |
| openSNP | rs764611160 |
| 23andMe | rs764611160 |
| SNPshot | rs764611160 |
| SNPdbe | rs764611160 |
| MSV3d | rs764611160 |
| GWAS Ctlg | rs764611160 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs764611160(-;-) |
| Alt | rs764611160(-;-) |
| Reference | Rs764611160(AG;AG) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | DLD |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000007.13:g.107556069_107556070delAG |
| CLNSRC | |
| CLNACC | RCV000482561.1, |
