rs1800560
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs1800560(A;A) |
| Make rs1800560(A;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 46373205 |
| Gene | CCR5, LOC102724297 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1800560 |
| dbSNP (classic) | rs1800560 |
| ClinGen | rs1800560 |
| ebi | rs1800560 |
| HLI | rs1800560 |
| Exac | rs1800560 |
| Gnomad | rs1800560 |
| Varsome | rs1800560 |
| LitVar | rs1800560 |
| Map | rs1800560 |
| PheGenI | rs1800560 |
| Biobank | rs1800560 |
| 1000 genomes | rs1800560 |
| hgdp | rs1800560 |
| ensembl | rs1800560 |
| geneview | rs1800560 |
| scholar | rs1800560 |
| rs1800560 | |
| pharmgkb | rs1800560 |
| gwascentral | rs1800560 |
| openSNP | rs1800560 |
| 23andMe | rs1800560 |
| SNPshot | rs1800560 |
| SNPdbe | rs1800560 |
| MSV3d | rs1800560 |
| GWAS Ctlg | rs1800560 |
| GMAF | 0.0 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs1800560(A;A) |
| Alt | rs1800560(A;A) |
| Reference | Rs1800560(T;T) |
| Significance | Other |
| Disease | Human immunodeficiency virus type 1 |
| Variation | info |
| Gene | LOC102724297 CCR5 |
| CLNDBN | Human immunodeficiency virus type 1, susceptibility to |
| Reversed | 0 |
| HGVS | NC_000003.11:g.46414696T>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000008670.3, |
