rs878852989
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs878852989(C;T) |
| Make rs878852989(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 21 |
| Position | 36756546 |
| Gene | HLCS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs878852989 |
| dbSNP (classic) | rs878852989 |
| ClinGen | rs878852989 |
| ebi | rs878852989 |
| HLI | rs878852989 |
| Exac | rs878852989 |
| Gnomad | rs878852989 |
| Varsome | rs878852989 |
| LitVar | rs878852989 |
| Map | rs878852989 |
| PheGenI | rs878852989 |
| Biobank | rs878852989 |
| 1000 genomes | rs878852989 |
| hgdp | rs878852989 |
| ensembl | rs878852989 |
| geneview | rs878852989 |
| scholar | rs878852989 |
| rs878852989 | |
| pharmgkb | rs878852989 |
| gwascentral | rs878852989 |
| openSNP | rs878852989 |
| 23andMe | rs878852989 |
| SNPshot | rs878852989 |
| SNPdbe | rs878852989 |
| MSV3d | rs878852989 |
| GWAS Ctlg | rs878852989 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs878852989(T;T) |
| Alt | rs878852989(T;T) |
| Reference | Rs878852989(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | HLCS |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000021.8:g.38128847G>A |
| CLNSRC | |
| CLNACC | RCV000224257.1, |
