rs260630
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| (T;T) | 0 | common in clinvar |
| Make rs260630(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 108910917 |
| Gene | EDAR, RANBP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs260630 |
| dbSNP (classic) | rs260630 |
| ClinGen | rs260630 |
| ebi | rs260630 |
| HLI | rs260630 |
| Exac | rs260630 |
| Gnomad | rs260630 |
| Varsome | rs260630 |
| LitVar | rs260630 |
| Map | rs260630 |
| PheGenI | rs260630 |
| Biobank | rs260630 |
| 1000 genomes | rs260630 |
| hgdp | rs260630 |
| ensembl | rs260630 |
| geneview | rs260630 |
| scholar | rs260630 |
| rs260630 | |
| pharmgkb | rs260630 |
| gwascentral | rs260630 |
| openSNP | rs260630 |
| 23andMe | rs260630 |
| SNPshot | rs260630 |
| SNPdbe | rs260630 |
| MSV3d | rs260630 |
| GWAS Ctlg | rs260630 |
| GMAF | 0.0652 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | Rs260630(C;C) |
| Alt | Rs260630(C;C) |
| Reference | Rs260630(T;T) |
| Significance | Unknown |
| Disease | not provided |
| Variation | info |
| Gene | EDAR |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000002.11:g.109527373A>G |
| CLNSRC | |
| CLNACC | RCV000143984.1, |
