rs2546890
From SNPedia
Associated with multiple sclerosis |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 1 | Higher risk of multiple sclerosis |
(A;G) | 1 | Higher risk of multiple sclerosis |
(G;G) | 1 | Lower risk of multiple sclerosis |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 159332892 |
Gene | LOC285626 |
is a | snp |
is | mentioned by |
dbSNP | rs2546890 |
dbSNP (classic) | rs2546890 |
ClinGen | rs2546890 |
ebi | rs2546890 |
HLI | rs2546890 |
Exac | rs2546890 |
Gnomad | rs2546890 |
Varsome | rs2546890 |
LitVar | rs2546890 |
Map | rs2546890 |
PheGenI | rs2546890 |
Biobank | rs2546890 |
1000 genomes | rs2546890 |
hgdp | rs2546890 |
ensembl | rs2546890 |
geneview | rs2546890 |
scholar | rs2546890 |
rs2546890 | |
pharmgkb | rs2546890 |
gwascentral | rs2546890 |
openSNP | rs2546890 |
23andMe | rs2546890 |
SNPshot | rs2546890 |
SNPdbe | rs2546890 |
MSV3d | rs2546890 |
GWAS Ctlg | rs2546890 |
GMAF | 0.4334 |
Max Magnitude | 1 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
23andMe blog multiple sclerosis rs2546890 IL12B G 0.87
GWAS snp | |
---|---|
PMID | [PMID 20953188] |
Trait | |
Title | Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2 |
Risk Allele | A |
P-val | 1E-20 |
Odds Ratio | 1.5400 [1.32-1.79] (Panel A) |
GWAS snp | |
---|---|
PMID | [PMID 22190364] |
Trait | |
Title | Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. |
Risk Allele | A |
P-val | 8E-8 |
Odds Ratio | 1.1600 None |
GWAS snp | |
---|---|
PMID | [PMID 21833088] |
Trait | |
Title | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
Risk Allele | A |
P-val | 1E-11 |
Odds Ratio | 1.1100 [1.10-1.13] |
[PMID 16600026] Asthma families show transmission disequilibrium of gene variants in the vitamin D metabolism and signalling pathway.
[PMID 19956101] Overview of the Rapid Response data.
[PMID 19956104] Evaluation of IL12B as a candidate type I diabetes susceptibility gene using data from the Type I Diabetes Genetics Consortium.
[PMID 23785401] Association of Genetic Markers with CSF Oligoclonal Bands in Multiple Sclerosis Patients
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 5
- Has genotype
- Has population
- 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 FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d