rs62620995
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs62620995(C;C) |
| Make rs62620995(C;T) |
| Make rs62620995(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 104355036 |
| Gene | DCSTAMP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs62620995 |
| dbSNP (classic) | rs62620995 |
| ClinGen | rs62620995 |
| ebi | rs62620995 |
| HLI | rs62620995 |
| Exac | rs62620995 |
| Gnomad | rs62620995 |
| Varsome | rs62620995 |
| LitVar | rs62620995 |
| Map | rs62620995 |
| PheGenI | rs62620995 |
| Biobank | rs62620995 |
| 1000 genomes | rs62620995 |
| hgdp | rs62620995 |
| ensembl | rs62620995 |
| geneview | rs62620995 |
| scholar | rs62620995 |
| rs62620995 | |
| pharmgkb | rs62620995 |
| gwascentral | rs62620995 |
| openSNP | rs62620995 |
| 23andMe | rs62620995 |
| SNPshot | rs62620995 |
| SNPdbe | rs62620995 |
| MSV3d | rs62620995 |
| GWAS Ctlg | rs62620995 |
| GMAF | 0.005969 |
| Max Magnitude | 0 |
[PMID 24370779] Identification of rare genetic variants in novel loci associated with Paget's disease of bone
