rs786201011
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (CT;CT) | 0 | common in clinvar |
| Make rs786201011(-;-) |
| Make rs786201011(-;CT) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 12 |
| Position | 12718213 |
| Gene | CDKN1B, GPR19 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs786201011 |
| dbSNP (classic) | rs786201011 |
| ClinGen | rs786201011 |
| ebi | rs786201011 |
| HLI | rs786201011 |
| Exac | rs786201011 |
| Gnomad | rs786201011 |
| Varsome | rs786201011 |
| LitVar | rs786201011 |
| Map | rs786201011 |
| PheGenI | rs786201011 |
| Biobank | rs786201011 |
| 1000 genomes | rs786201011 |
| hgdp | rs786201011 |
| ensembl | rs786201011 |
| geneview | rs786201011 |
| scholar | rs786201011 |
| rs786201011 | |
| pharmgkb | rs786201011 |
| gwascentral | rs786201011 |
| openSNP | rs786201011 |
| 23andMe | rs786201011 |
| SNPshot | rs786201011 |
| SNPdbe | rs786201011 |
| MSV3d | rs786201011 |
| GWAS Ctlg | rs786201011 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs786201011(-;-) |
| Alt | rs786201011(-;-) |
| Reference | Rs786201011(CT;CT) |
| Significance | Pathogenic |
| Disease | Multiple endocrine neoplasia |
| Variation | info |
| Gene | LOC101929220 CDKN1B |
| CLNDBN | Multiple endocrine neoplasia, type 4 |
| Reversed | 0 |
| HGVS | NC_000012.11:g.12871147_12871148delCT |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000162209.3, |
