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