rs772213710
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs772213710(C;T) |
| Make rs772213710(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 18 |
| Position | 60372069 |
| Gene | MC4R |
| is a | snp |
| is | mentioned by |
| dbSNP | rs772213710 |
| dbSNP (classic) | rs772213710 |
| ClinGen | rs772213710 |
| ebi | rs772213710 |
| HLI | rs772213710 |
| Exac | rs772213710 |
| Gnomad | rs772213710 |
| Varsome | rs772213710 |
| LitVar | rs772213710 |
| Map | rs772213710 |
| PheGenI | rs772213710 |
| Biobank | rs772213710 |
| 1000 genomes | rs772213710 |
| hgdp | rs772213710 |
| ensembl | rs772213710 |
| geneview | rs772213710 |
| scholar | rs772213710 |
| rs772213710 | |
| pharmgkb | rs772213710 |
| gwascentral | rs772213710 |
| openSNP | rs772213710 |
| 23andMe | rs772213710 |
| SNPshot | rs772213710 |
| SNPdbe | rs772213710 |
| MSV3d | rs772213710 |
| GWAS Ctlg | rs772213710 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs772213710(T;T) |
| Alt | rs772213710(T;T) |
| Reference | Rs772213710(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | MC4R |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000018.9:g.58039302C>T |
| CLNSRC | |
| CLNACC | RCV000432683.1, |
