rs747681609
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs747681609(C;T) |
| Make rs747681609(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 18 |
| Position | 60371856 |
| Gene | MC4R |
| is a | snp |
| is | mentioned by |
| dbSNP | rs747681609 |
| dbSNP (classic) | rs747681609 |
| ClinGen | rs747681609 |
| ebi | rs747681609 |
| HLI | rs747681609 |
| Exac | rs747681609 |
| Gnomad | rs747681609 |
| Varsome | rs747681609 |
| LitVar | rs747681609 |
| Map | rs747681609 |
| PheGenI | rs747681609 |
| Biobank | rs747681609 |
| 1000 genomes | rs747681609 |
| hgdp | rs747681609 |
| ensembl | rs747681609 |
| geneview | rs747681609 |
| scholar | rs747681609 |
| rs747681609 | |
| pharmgkb | rs747681609 |
| gwascentral | rs747681609 |
| openSNP | rs747681609 |
| 23andMe | rs747681609 |
| SNPshot | rs747681609 |
| SNPdbe | rs747681609 |
| MSV3d | rs747681609 |
| GWAS Ctlg | rs747681609 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs747681609(T;T) |
| Alt | rs747681609(T;T) |
| Reference | Rs747681609(C;C) |
| Significance | Probable-Pathogenic |
| Disease | Obesity |
| Variation | info |
| Gene | MC4R |
| CLNDBN | Obesity |
| Reversed | 0 |
| HGVS | NC_000018.9:g.58039089C>T |
| CLNSRC | Illumina |
| CLNACC | RCV000332082.1, |
