rs141178995
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs141178995(C;C) |
| Make rs141178995(C;G) |
| Make rs141178995(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 11 |
| Position | 68426112 |
| Gene | LRP5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs141178995 |
| dbSNP (classic) | rs141178995 |
| ClinGen | rs141178995 |
| ebi | rs141178995 |
| HLI | rs141178995 |
| Exac | rs141178995 |
| Gnomad | rs141178995 |
| Varsome | rs141178995 |
| LitVar | rs141178995 |
| Map | rs141178995 |
| PheGenI | rs141178995 |
| Biobank | rs141178995 |
| 1000 genomes | rs141178995 |
| hgdp | rs141178995 |
| ensembl | rs141178995 |
| geneview | rs141178995 |
| scholar | rs141178995 |
| rs141178995 | |
| pharmgkb | rs141178995 |
| gwascentral | rs141178995 |
| openSNP | rs141178995 |
| 23andMe | rs141178995 |
| SNPshot | rs141178995 |
| SNPdbe | rs141178995 |
| MSV3d | rs141178995 |
| GWAS Ctlg | rs141178995 |
| Max Magnitude | 0 |
OMIM pathogenic variant
