rs376664522
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs376664522(A;A) |
| Make rs376664522(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 219212413 |
| Gene | ABCB6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs376664522 |
| dbSNP (classic) | rs376664522 |
| ClinGen | rs376664522 |
| ebi | rs376664522 |
| HLI | rs376664522 |
| Exac | rs376664522 |
| Gnomad | rs376664522 |
| Varsome | rs376664522 |
| LitVar | rs376664522 |
| Map | rs376664522 |
| PheGenI | rs376664522 |
| Biobank | rs376664522 |
| 1000 genomes | rs376664522 |
| hgdp | rs376664522 |
| ensembl | rs376664522 |
| geneview | rs376664522 |
| scholar | rs376664522 |
| rs376664522 | |
| pharmgkb | rs376664522 |
| gwascentral | rs376664522 |
| openSNP | rs376664522 |
| 23andMe | rs376664522 |
| SNPshot | rs376664522 |
| SNPdbe | rs376664522 |
| MSV3d | rs376664522 |
| GWAS Ctlg | rs376664522 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs376664522(A;A) |
| Alt | rs376664522(A;A) |
| Reference | Rs376664522(G;G) |
| Significance | Other |
| Disease | Langereis blood group |
| Variation | info |
| Gene | ABCB6 |
| CLNDBN | Langereis blood group |
| Reversed | 0 |
| HGVS | NC_000002.11:g.220077135G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000023436.3, |
