rs776975632
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs776975632(C;C) |
| Make rs776975632(C;T) |
| Make rs776975632(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 16 |
| Position | 68828254 |
| Gene | CDH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs776975632 |
| dbSNP (classic) | rs776975632 |
| ClinGen | rs776975632 |
| ebi | rs776975632 |
| HLI | rs776975632 |
| Exac | rs776975632 |
| Gnomad | rs776975632 |
| Varsome | rs776975632 |
| LitVar | rs776975632 |
| Map | rs776975632 |
| PheGenI | rs776975632 |
| Biobank | rs776975632 |
| 1000 genomes | rs776975632 |
| hgdp | rs776975632 |
| ensembl | rs776975632 |
| geneview | rs776975632 |
| scholar | rs776975632 |
| rs776975632 | |
| pharmgkb | rs776975632 |
| gwascentral | rs776975632 |
| openSNP | rs776975632 |
| 23andMe | rs776975632 |
| SNPshot | rs776975632 |
| SNPdbe | rs776975632 |
| MSV3d | rs776975632 |
| GWAS Ctlg | rs776975632 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs776975632(T;T) |
| Alt | rs776975632(T;T) |
| Reference | rs776975632(C;C) |
| Significance | Unknown |
| Disease | not specified |
| Variation | info |
| Gene | CDH1 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000016.9:g.68862157C>T |
| CLNSRC | |
| CLNACC | RCV000479819.1, |
