rs8187797
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Reference | GRCh38 38.1/142 |
| Chromosome | 7 |
| Position | 87439814 |
| Gene | ABCB4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8187797 |
| dbSNP (classic) | rs8187797 |
| ClinGen | rs8187797 |
| ebi | rs8187797 |
| HLI | rs8187797 |
| Exac | rs8187797 |
| Gnomad | rs8187797 |
| Varsome | rs8187797 |
| LitVar | rs8187797 |
| Map | rs8187797 |
| PheGenI | rs8187797 |
| Biobank | rs8187797 |
| 1000 genomes | rs8187797 |
| hgdp | rs8187797 |
| ensembl | rs8187797 |
| geneview | rs8187797 |
| scholar | rs8187797 |
| rs8187797 | |
| pharmgkb | rs8187797 |
| gwascentral | rs8187797 |
| openSNP | rs8187797 |
| 23andMe | rs8187797 |
| SNPshot | rs8187797 |
| SNPdbe | rs8187797 |
| MSV3d | rs8187797 |
| GWAS Ctlg | rs8187797 |
| Max Magnitude | 0 |
[PMID 25802476
] The Affymetrix DMET Plus Platform Reveals Unique Distribution of ADME-Related Variants in Ethnic Arabs
| ClinVar | |
|---|---|
| Risk | rs8187797(G;G) |
| Alt | rs8187797(G;G) |
| Reference | Rs8187797(C;C) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | ABCB4 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000007.13:g.87069130C>G |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000174682.2, |
