rs8111998
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8111998(C;C) |
| Make rs8111998(C;T) |
| Make rs8111998(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 22558873 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8111998 |
| dbSNP (classic) | rs8111998 |
| ClinGen | rs8111998 |
| ebi | rs8111998 |
| HLI | rs8111998 |
| Exac | rs8111998 |
| Gnomad | rs8111998 |
| Varsome | rs8111998 |
| LitVar | rs8111998 |
| Map | rs8111998 |
| PheGenI | rs8111998 |
| Biobank | rs8111998 |
| 1000 genomes | rs8111998 |
| hgdp | rs8111998 |
| ensembl | rs8111998 |
| geneview | rs8111998 |
| scholar | rs8111998 |
| rs8111998 | |
| pharmgkb | rs8111998 |
| gwascentral | rs8111998 |
| openSNP | rs8111998 |
| 23andMe | rs8111998 |
| SNPshot | rs8111998 |
| SNPdbe | rs8111998 |
| MSV3d | rs8111998 |
| GWAS Ctlg | rs8111998 |
| GMAF | 0.2218 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21979947 ]
|
| Trait | |
| Title | A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries. |
| Risk Allele | |
| P-val | 8E-7 |
| Odds Ratio | 1.7100 [NR] |
