rs724159826
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs724159826(C;C) |
| Make rs724159826(C;G) |
| Make rs724159826(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 11 |
| Position | 68448809 |
| Gene | LRP5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs724159826 |
| dbSNP (classic) | rs724159826 |
| ClinGen | rs724159826 |
| ebi | rs724159826 |
| HLI | rs724159826 |
| Exac | rs724159826 |
| Gnomad | rs724159826 |
| Varsome | rs724159826 |
| LitVar | rs724159826 |
| Map | rs724159826 |
| PheGenI | rs724159826 |
| Biobank | rs724159826 |
| 1000 genomes | rs724159826 |
| hgdp | rs724159826 |
| ensembl | rs724159826 |
| geneview | rs724159826 |
| scholar | rs724159826 |
| rs724159826 | |
| pharmgkb | rs724159826 |
| gwascentral | rs724159826 |
| openSNP | rs724159826 |
| 23andMe | rs724159826 |
| SNPshot | rs724159826 |
| SNPdbe | rs724159826 |
| MSV3d | rs724159826 |
| GWAS Ctlg | rs724159826 |
| Max Magnitude | 0 |
aka NM_002335.3(LRP5):c.4587G>C or (p.Arg1529Ser)
OMIM pathogenic variant
