rs2664156
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2664156(C;C) |
| Make rs2664156(C;T) |
| Make rs2664156(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 19 |
| Position | 50873907 |
| Gene | KLK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2664156 |
| dbSNP (classic) | rs2664156 |
| ClinGen | rs2664156 |
| ebi | rs2664156 |
| HLI | rs2664156 |
| Exac | rs2664156 |
| Gnomad | rs2664156 |
| Varsome | rs2664156 |
| LitVar | rs2664156 |
| Map | rs2664156 |
| PheGenI | rs2664156 |
| Biobank | rs2664156 |
| 1000 genomes | rs2664156 |
| hgdp | rs2664156 |
| ensembl | rs2664156 |
| geneview | rs2664156 |
| scholar | rs2664156 |
| rs2664156 | |
| pharmgkb | rs2664156 |
| gwascentral | rs2664156 |
| openSNP | rs2664156 |
| 23andMe | rs2664156 |
| SNPshot | rs2664156 |
| SNPdbe | rs2664156 |
| MSV3d | rs2664156 |
| GWAS Ctlg | rs2664156 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23936387 ]
|
| Trait | Celiac disease |
| Title | A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease. |
| Risk Allele | C |
| P-val | 6E-6 |
| Odds Ratio | NR NR |
