rs11575892
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs11575892(C;T) |
| Make rs11575892(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 67483152 |
| Gene | AGRP, ATP6V0D1, LOC101927837 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11575892 |
| dbSNP (classic) | rs11575892 |
| ClinGen | rs11575892 |
| ebi | rs11575892 |
| HLI | rs11575892 |
| Exac | rs11575892 |
| Gnomad | rs11575892 |
| Varsome | rs11575892 |
| LitVar | rs11575892 |
| Map | rs11575892 |
| PheGenI | rs11575892 |
| Biobank | rs11575892 |
| 1000 genomes | rs11575892 |
| hgdp | rs11575892 |
| ensembl | rs11575892 |
| geneview | rs11575892 |
| scholar | rs11575892 |
| rs11575892 | |
| pharmgkb | rs11575892 |
| gwascentral | rs11575892 |
| openSNP | rs11575892 |
| 23andMe | rs11575892 |
| SNPshot | rs11575892 |
| SNPdbe | rs11575892 |
| MSV3d | rs11575892 |
| GWAS Ctlg | rs11575892 |
| GMAF | 0.01837 |
| Max Magnitude | 0 |
[PMID 19602223
] Association between a rare SNP in the second intron of human Agouti related protein gene and increased BMI
