rs373910016
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs373910016(A;A) |
| Make rs373910016(A;G) |
| Make rs373910016(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 11 |
| Position | 68386660 |
| Gene | LRP5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs373910016 |
| dbSNP (classic) | rs373910016 |
| ClinGen | rs373910016 |
| ebi | rs373910016 |
| HLI | rs373910016 |
| Exac | rs373910016 |
| Gnomad | rs373910016 |
| Varsome | rs373910016 |
| LitVar | rs373910016 |
| Map | rs373910016 |
| PheGenI | rs373910016 |
| Biobank | rs373910016 |
| 1000 genomes | rs373910016 |
| hgdp | rs373910016 |
| ensembl | rs373910016 |
| geneview | rs373910016 |
| scholar | rs373910016 |
| rs373910016 | |
| pharmgkb | rs373910016 |
| gwascentral | rs373910016 |
| openSNP | rs373910016 |
| 23andMe | rs373910016 |
| SNPshot | rs373910016 |
| SNPdbe | rs373910016 |
| MSV3d | rs373910016 |
| GWAS Ctlg | rs373910016 |
| Max Magnitude | 0 |
aka NM_002335.3(LRP5):c.1360G>A or (p.Val454Met)
OMIM pathogenic variant
