rs10249788
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10249788(C;C) |
| Make rs10249788(C;T) |
| Make rs10249788(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 17298523 |
| Gene | AHR, LOC101927609 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10249788 |
| dbSNP (classic) | rs10249788 |
| ClinGen | rs10249788 |
| ebi | rs10249788 |
| HLI | rs10249788 |
| Exac | rs10249788 |
| Gnomad | rs10249788 |
| Varsome | rs10249788 |
| LitVar | rs10249788 |
| Map | rs10249788 |
| PheGenI | rs10249788 |
| Biobank | rs10249788 |
| 1000 genomes | rs10249788 |
| hgdp | rs10249788 |
| ensembl | rs10249788 |
| geneview | rs10249788 |
| scholar | rs10249788 |
| rs10249788 | |
| pharmgkb | rs10249788 |
| gwascentral | rs10249788 |
| openSNP | rs10249788 |
| 23andMe | rs10249788 |
| SNPshot | rs10249788 |
| SNPdbe | rs10249788 |
| MSV3d | rs10249788 |
| GWAS Ctlg | rs10249788 |
| GMAF | 0.2475 |
| Max Magnitude | 0 |
[PMID 23208493] Inhibition of AHR transcription by NF1C is affected by a single-nucleotide polymorphism, and is involved in suppression of human uterine endometrial cancer
[PMID 22211302] The association of functional polymorphisms in the aryl hydrocarbon receptor (AHR) gene with the risk of vitiligo in Han Chinese populations.
[PMID 29325309] [Association of Crohn's disease with aryl hydrocarbon receptor gene polymorphisms and haplotypes].
