rs1007190
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1007190(C;C) |
| Make rs1007190(C;T) |
| Make rs1007190(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 44960841 |
| Gene | C1QL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1007190 |
| dbSNP (classic) | rs1007190 |
| ClinGen | rs1007190 |
| ebi | rs1007190 |
| HLI | rs1007190 |
| Exac | rs1007190 |
| Gnomad | rs1007190 |
| Varsome | rs1007190 |
| LitVar | rs1007190 |
| Map | rs1007190 |
| PheGenI | rs1007190 |
| Biobank | rs1007190 |
| 1000 genomes | rs1007190 |
| hgdp | rs1007190 |
| ensembl | rs1007190 |
| geneview | rs1007190 |
| scholar | rs1007190 |
| rs1007190 | |
| pharmgkb | rs1007190 |
| gwascentral | rs1007190 |
| openSNP | rs1007190 |
| 23andMe | rs1007190 |
| SNPshot | rs1007190 |
| SNPdbe | rs1007190 |
| MSV3d | rs1007190 |
| GWAS Ctlg | rs1007190 |
| GMAF | 0.1492 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23725790] |
| Trait | DNA methylation (variation) |
| Title | GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association. |
| Risk Allele | T |
| P-val | 2E-6 |
| Odds Ratio | NR NR |
