rs12444979
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12444979(C;C) |
| Make rs12444979(C;T) |
| Make rs12444979(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 19922278 |
| Gene | LOC105371116 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12444979 |
| dbSNP (classic) | rs12444979 |
| ClinGen | rs12444979 |
| ebi | rs12444979 |
| HLI | rs12444979 |
| Exac | rs12444979 |
| Gnomad | rs12444979 |
| Varsome | rs12444979 |
| LitVar | rs12444979 |
| Map | rs12444979 |
| PheGenI | rs12444979 |
| Biobank | rs12444979 |
| 1000 genomes | rs12444979 |
| hgdp | rs12444979 |
| ensembl | rs12444979 |
| geneview | rs12444979 |
| scholar | rs12444979 |
| rs12444979 | |
| pharmgkb | rs12444979 |
| gwascentral | rs12444979 |
| openSNP | rs12444979 |
| 23andMe | rs12444979 |
| SNPshot | rs12444979 |
| SNPdbe | rs12444979 |
| MSV3d | rs12444979 |
| GWAS Ctlg | rs12444979 |
| GMAF | 0.07254 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20935630 ]
|
| Trait | |
| Title | Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index |
| Risk Allele | C |
| P-val | 3E-21 |
| Odds Ratio | 0.17 [0.11-0.23] kg/m2 increase |
[PMID 22391884] Ethnic differentiation of copy number variation on chromosome 16p12.3 for association with obesity phenotypes in European and Chinese populations.
[PMID 23471855] The genetics of childhood obesity and interaction with dietary macronutrients.
[PMID 27282283] UGT2B4 previously implicated in the risk of breast cancer is associated with menarche timing in ukrainian females.
