rs1800571
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs1800571(A;A) |
| Make rs1800571(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 12381349 |
| Gene | PPARG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1800571 |
| dbSNP (classic) | rs1800571 |
| ClinGen | rs1800571 |
| ebi | rs1800571 |
| HLI | rs1800571 |
| Exac | rs1800571 |
| Gnomad | rs1800571 |
| Varsome | rs1800571 |
| LitVar | rs1800571 |
| Map | rs1800571 |
| PheGenI | rs1800571 |
| Biobank | rs1800571 |
| 1000 genomes | rs1800571 |
| hgdp | rs1800571 |
| ensembl | rs1800571 |
| geneview | rs1800571 |
| scholar | rs1800571 |
| rs1800571 | |
| pharmgkb | rs1800571 |
| gwascentral | rs1800571 |
| openSNP | rs1800571 |
| 23andMe | rs1800571 |
| SNPshot | rs1800571 |
| SNPdbe | rs1800571 |
| MSV3d | rs1800571 |
| GWAS Ctlg | rs1800571 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs1800571(A;A) |
| Alt | rs1800571(A;A) |
| Reference | Rs1800571(C;C) |
| Significance | Pathogenic |
| Disease | Morbid obesity |
| Variation | info |
| Gene | PPARG |
| CLNDBN | Morbid obesity |
| Reversed | 0 |
| HGVS | NC_000003.11:g.12422848C>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000008603.3, |
[PMID 16783862] PPAR-gamma gene polymorphisms and psoriatic arthritis.
[PMID 19139070
] Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.
