rs140207606
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common genotype |
| Make rs140207606(A;A) |
| Make rs140207606(A;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 4 |
| Position | 88118244 |
| Gene | ABCG2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs140207606 |
| dbSNP (classic) | rs140207606 |
| ClinGen | rs140207606 |
| ebi | rs140207606 |
| HLI | rs140207606 |
| Exac | rs140207606 |
| Gnomad | rs140207606 |
| Varsome | rs140207606 |
| LitVar | rs140207606 |
| Map | rs140207606 |
| PheGenI | rs140207606 |
| Biobank | rs140207606 |
| 1000 genomes | rs140207606 |
| hgdp | rs140207606 |
| ensembl | rs140207606 |
| geneview | rs140207606 |
| scholar | rs140207606 |
| rs140207606 | |
| pharmgkb | rs140207606 |
| gwascentral | rs140207606 |
| openSNP | rs140207606 |
| 23andMe | rs140207606 |
| SNPshot | rs140207606 |
| SNPdbe | rs140207606 |
| MSV3d | rs140207606 |
| GWAS Ctlg | rs140207606 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs140207606(A;A) rs140207606(T;T) |
| Alt | rs140207606(A;A) rs140207606(T;T) |
| Reference | Rs140207606(G;G) |
| Significance | Other |
| Disease | Blood group |
| Variation | info |
| Gene | ABCG2 |
| CLNDBN | Blood group, Junior system |
| Reversed | 0 |
| HGVS | NC_000004.11:g.89039396G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000023339.2, |
