rs149645175
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs149645175(C;G) |
| Make rs149645175(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 68448822 |
| Gene | LRP5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs149645175 |
| dbSNP (classic) | rs149645175 |
| ClinGen | rs149645175 |
| ebi | rs149645175 |
| HLI | rs149645175 |
| Exac | rs149645175 |
| Gnomad | rs149645175 |
| Varsome | rs149645175 |
| LitVar | rs149645175 |
| Map | rs149645175 |
| PheGenI | rs149645175 |
| Biobank | rs149645175 |
| 1000 genomes | rs149645175 |
| hgdp | rs149645175 |
| ensembl | rs149645175 |
| geneview | rs149645175 |
| scholar | rs149645175 |
| rs149645175 | |
| pharmgkb | rs149645175 |
| gwascentral | rs149645175 |
| openSNP | rs149645175 |
| 23andMe | rs149645175 |
| SNPshot | rs149645175 |
| SNPdbe | rs149645175 |
| MSV3d | rs149645175 |
| GWAS Ctlg | rs149645175 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs149645175(G;G) rs149645175(T;T) |
| Alt | rs149645175(G;G) rs149645175(T;T) |
| Reference | Rs149645175(C;C) |
| Significance | Pathogenic |
| Disease | Osteoporosis with pseudoglioma |
| Variation | info |
| Gene | LRP5 |
| CLNDBN | Osteoporosis with pseudoglioma |
| Reversed | 0 |
| HGVS | NC_000011.9:g.68216290C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000033260.4, |
