rs1926736
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1926736(C;C) |
| Make rs1926736(C;T) |
| Make rs1926736(T;T) |
| Reference | GRCh37.p5 37.3/137 |
| Chromosome | 10 |
| Position | 17891705 |
| Gene | BAHD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1926736 |
| dbSNP (classic) | rs1926736 |
| ClinGen | rs1926736 |
| ebi | rs1926736 |
| HLI | rs1926736 |
| Exac | rs1926736 |
| Gnomad | rs1926736 |
| Varsome | rs1926736 |
| LitVar | rs1926736 |
| Map | rs1926736 |
| PheGenI | rs1926736 |
| Biobank | rs1926736 |
| 1000 genomes | rs1926736 |
| hgdp | rs1926736 |
| ensembl | rs1926736 |
| geneview | rs1926736 |
| scholar | rs1926736 |
| rs1926736 | |
| pharmgkb | rs1926736 |
| gwascentral | rs1926736 |
| openSNP | rs1926736 |
| 23andMe | rs1926736 |
| SNPshot | rs1926736 |
| SNPdbe | rs1926736 |
| MSV3d | rs1926736 |
| GWAS Ctlg | rs1926736 |
| GMAF | 0.4169 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19902202] Genetic variants in the mannose receptor gene (MRC1) are associated with asthma in two independent populations
[PMID 16385451
] A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.
[PMID 22392581] Genetic variants of the MRC1 gene and the IFNG gene are associated with leprosy in Han Chinese from Southwest China.
