rs878853002
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs878853002(A;A) |
| Make rs878853002(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 17 |
| Position | 44255272 |
| Gene | SLC4A1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs878853002 |
| dbSNP (classic) | rs878853002 |
| ClinGen | rs878853002 |
| ebi | rs878853002 |
| HLI | rs878853002 |
| Exac | rs878853002 |
| Gnomad | rs878853002 |
| Varsome | rs878853002 |
| LitVar | rs878853002 |
| Map | rs878853002 |
| PheGenI | rs878853002 |
| Biobank | rs878853002 |
| 1000 genomes | rs878853002 |
| hgdp | rs878853002 |
| ensembl | rs878853002 |
| geneview | rs878853002 |
| scholar | rs878853002 |
| rs878853002 | |
| pharmgkb | rs878853002 |
| gwascentral | rs878853002 |
| openSNP | rs878853002 |
| 23andMe | rs878853002 |
| SNPshot | rs878853002 |
| SNPdbe | rs878853002 |
| MSV3d | rs878853002 |
| GWAS Ctlg | rs878853002 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs878853002(A;A) |
| Alt | rs878853002(A;A) |
| Reference | Rs878853002(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | SLC4A1 |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000017.10:g.42332640C>T |
| CLNSRC | |
| CLNACC | RCV000224119.1, |
