rs830998
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs830998(A;A) |
| Make rs830998(A;C) |
| Make rs830998(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 169276576 |
| Gene | LRP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs830998 |
| dbSNP (classic) | rs830998 |
| ClinGen | rs830998 |
| ebi | rs830998 |
| HLI | rs830998 |
| Exac | rs830998 |
| Gnomad | rs830998 |
| Varsome | rs830998 |
| LitVar | rs830998 |
| Map | rs830998 |
| PheGenI | rs830998 |
| Biobank | rs830998 |
| 1000 genomes | rs830998 |
| hgdp | rs830998 |
| ensembl | rs830998 |
| geneview | rs830998 |
| scholar | rs830998 |
| rs830998 | |
| pharmgkb | rs830998 |
| gwascentral | rs830998 |
| openSNP | rs830998 |
| 23andMe | rs830998 |
| SNPshot | rs830998 |
| SNPdbe | rs830998 |
| MSV3d | rs830998 |
| GWAS Ctlg | rs830998 |
| GMAF | 0.1621 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21079607 ]
|
| Trait | |
| Title | A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa |
| Risk Allele | |
| P-val | 0.000009 |
| Odds Ratio | None None |
