rs3820198
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3820198(G;G) |
| Make rs3820198(G;T) |
| Make rs3820198(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 53326979 |
| Gene | LINC01771, LRP8 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3820198 |
| dbSNP (classic) | rs3820198 |
| ClinGen | rs3820198 |
| ebi | rs3820198 |
| HLI | rs3820198 |
| Exac | rs3820198 |
| Gnomad | rs3820198 |
| Varsome | rs3820198 |
| LitVar | rs3820198 |
| Map | rs3820198 |
| PheGenI | rs3820198 |
| Biobank | rs3820198 |
| 1000 genomes | rs3820198 |
| hgdp | rs3820198 |
| ensembl | rs3820198 |
| geneview | rs3820198 |
| scholar | rs3820198 |
| rs3820198 | |
| pharmgkb | rs3820198 |
| gwascentral | rs3820198 |
| openSNP | rs3820198 |
| 23andMe | rs3820198 |
| SNPshot | rs3820198 |
| SNPdbe | rs3820198 |
| MSV3d | rs3820198 |
| GWAS Ctlg | rs3820198 |
| GMAF | 0.4789 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21316997] Investigation of LRP8 gene in 1p31 QTL linked to LDL peak particle diameter in the Quebec family study
[PMID 17847002
] An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction.
[PMID 22889673] Association analysis of LRP8 SNP rs3820198 and rs5174 with Parkinson's disease in Han Chinese population.
