rs1290349
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1290349(A;A) |
| Make rs1290349(A;C) |
| Make rs1290349(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 112166831 |
| Gene | LOC107987164, TEX12 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1290349 |
| dbSNP (classic) | rs1290349 |
| ClinGen | rs1290349 |
| ebi | rs1290349 |
| HLI | rs1290349 |
| Exac | rs1290349 |
| Gnomad | rs1290349 |
| Varsome | rs1290349 |
| LitVar | rs1290349 |
| Map | rs1290349 |
| PheGenI | rs1290349 |
| Biobank | rs1290349 |
| 1000 genomes | rs1290349 |
| hgdp | rs1290349 |
| ensembl | rs1290349 |
| geneview | rs1290349 |
| scholar | rs1290349 |
| rs1290349 | |
| pharmgkb | rs1290349 |
| gwascentral | rs1290349 |
| openSNP | rs1290349 |
| 23andMe | rs1290349 |
| SNPshot | rs1290349 |
| SNPdbe | rs1290349 |
| MSV3d | rs1290349 |
| GWAS Ctlg | rs1290349 |
| GMAF | 0.2287 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
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| ||
[PMID 22837141] Joint analysis of SNPs and proteins identifies regulatory IL18 gene variations decreasing the chance of spastic cerebral palsy
