rs6744682
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6744682(A;A) |
| Make rs6744682(A;T) |
| Make rs6744682(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 11789202 |
| Gene | LPIN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6744682 |
| dbSNP (classic) | rs6744682 |
| ClinGen | rs6744682 |
| ebi | rs6744682 |
| HLI | rs6744682 |
| Exac | rs6744682 |
| Gnomad | rs6744682 |
| Varsome | rs6744682 |
| LitVar | rs6744682 |
| Map | rs6744682 |
| PheGenI | rs6744682 |
| Biobank | rs6744682 |
| 1000 genomes | rs6744682 |
| hgdp | rs6744682 |
| ensembl | rs6744682 |
| geneview | rs6744682 |
| scholar | rs6744682 |
| rs6744682 | |
| pharmgkb | rs6744682 |
| gwascentral | rs6744682 |
| openSNP | rs6744682 |
| 23andMe | rs6744682 |
| SNPshot | rs6744682 |
| SNPdbe | rs6744682 |
| MSV3d | rs6744682 |
| GWAS Ctlg | rs6744682 |
| GMAF | 0.359 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20356931] Studies of association between LPIN1 variants and common metabolic phenotypes among 17,538 Danes
[PMID 18591397
] Evaluating the role of LPIN1 variation in insulin resistance, body weight, and human lipodystrophy in U.K. Populations.
