rs56163822
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs56163822(G;T) |
| Make rs56163822(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 100493323 |
| Gene | NR1H4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs56163822 |
| dbSNP (classic) | rs56163822 |
| ClinGen | rs56163822 |
| ebi | rs56163822 |
| HLI | rs56163822 |
| Exac | rs56163822 |
| Gnomad | rs56163822 |
| Varsome | rs56163822 |
| LitVar | rs56163822 |
| Map | rs56163822 |
| PheGenI | rs56163822 |
| Biobank | rs56163822 |
| 1000 genomes | rs56163822 |
| hgdp | rs56163822 |
| ensembl | rs56163822 |
| geneview | rs56163822 |
| scholar | rs56163822 |
| rs56163822 | |
| pharmgkb | rs56163822 |
| gwascentral | rs56163822 |
| openSNP | rs56163822 |
| 23andMe | rs56163822 |
| SNPshot | rs56163822 |
| SNPdbe | rs56163822 |
| MSV3d | rs56163822 |
| GWAS Ctlg | rs56163822 |
| GMAF | 0.06795 |
| Max Magnitude | 0 |
[PMID 22929053
] Association of genetic variation in the NR1H4 gene, encoding the nuclear bile acid receptor FXR, with inflammatory bowel disease
| ClinVar | |
|---|---|
| Risk | rs56163822(T;T) |
| Alt | rs56163822(T;T) |
| Reference | Rs56163822(G;G) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | NR1H4 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000012.11:g.100887101G>T |
| CLNSRC | |
| CLNACC | RCV000242576.2, |
[PMID 31062417] Impact of farnesoid X receptor SNPs on hepatic decompensation and mortality in cirrhotic patients with portal hypertension.
