rs12368653
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12368653(A;A) |
| Make rs12368653(A;G) |
| Make rs12368653(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 57739473 |
| Gene | AGAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12368653 |
| dbSNP (classic) | rs12368653 |
| ClinGen | rs12368653 |
| ebi | rs12368653 |
| HLI | rs12368653 |
| Exac | rs12368653 |
| Gnomad | rs12368653 |
| Varsome | rs12368653 |
| LitVar | rs12368653 |
| Map | rs12368653 |
| PheGenI | rs12368653 |
| Biobank | rs12368653 |
| 1000 genomes | rs12368653 |
| hgdp | rs12368653 |
| ensembl | rs12368653 |
| geneview | rs12368653 |
| scholar | rs12368653 |
| rs12368653 | |
| pharmgkb | rs12368653 |
| gwascentral | rs12368653 |
| openSNP | rs12368653 |
| 23andMe | rs12368653 |
| SNPshot | rs12368653 |
| SNPdbe | rs12368653 |
| MSV3d | rs12368653 |
| GWAS Ctlg | rs12368653 |
| GMAF | 0.3168 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19525955] Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
[PMID 20405052
] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.
| GWAS snp | |
|---|---|
| PMID | [PMID 21833088 |
| Trait | Multiple sclerosis |
| Title | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
| Risk Allele | A |
| P-val | 2E-9 |
| Odds Ratio | 1.10 [1.09-1.12] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 12
- Has genotype
- Has population
- Uses omim
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
