rs1799999
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | normal risk |
| (G;T) | ||
| (T;T) | 3 | insulin resistance |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 113878379 |
| Gene | PPP1R3A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1799999 |
| dbSNP (classic) | rs1799999 |
| ClinGen | rs1799999 |
| ebi | rs1799999 |
| HLI | rs1799999 |
| Exac | rs1799999 |
| Gnomad | rs1799999 |
| Varsome | rs1799999 |
| LitVar | rs1799999 |
| Map | rs1799999 |
| PheGenI | rs1799999 |
| Biobank | rs1799999 |
| 1000 genomes | rs1799999 |
| hgdp | rs1799999 |
| ensembl | rs1799999 |
| geneview | rs1799999 |
| scholar | rs1799999 |
| rs1799999 | |
| pharmgkb | rs1799999 |
| gwascentral | rs1799999 |
| openSNP | rs1799999 |
| 23andMe | rs1799999 |
| SNPshot | rs1799999 |
| SNPdbe | rs1799999 |
| MSV3d | rs1799999 |
| GWAS Ctlg | rs1799999 |
| GMAF | 0.2911 |
| Max Magnitude | 3 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | Rs1799999(T;T) |
| Alt | Rs1799999(T;T) |
| Reference | Rs1799999(G;G) |
| Significance | Other |
| Disease | Insulin resistance |
| Variation | info |
| Gene | PPP1R3A |
| CLNDBN | Insulin resistance, susceptibility to |
| Reversed | 1 |
| HGVS | NC_000007.13:g.113518434C>A |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000009243.2, |
[PMID 18853455
] Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson disease.
[PMID 23133645] The Interactive Effect of SIRT1 Promoter Region Polymorphism on Type 2 Diabetes Susceptibility in the North Indian Population
