rs874628
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs874628(C;C) |
Make rs874628(C;T) |
Make rs874628(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 18193890 |
Gene | MPV17L2 |
is a | snp |
is | mentioned by |
dbSNP | rs874628 |
dbSNP (classic) | rs874628 |
ClinGen | rs874628 |
ebi | rs874628 |
HLI | rs874628 |
Exac | rs874628 |
Gnomad | rs874628 |
Varsome | rs874628 |
LitVar | rs874628 |
Map | rs874628 |
PheGenI | rs874628 |
Biobank | rs874628 |
1000 genomes | rs874628 |
hgdp | rs874628 |
ensembl | rs874628 |
geneview | rs874628 |
scholar | rs874628 |
rs874628 | |
pharmgkb | rs874628 |
gwascentral | rs874628 |
openSNP | rs874628 |
23andMe | rs874628 |
SNPshot | rs874628 |
SNPdbe | rs874628 |
MSV3d | rs874628 |
GWAS Ctlg | rs874628 |
GMAF | 0.1919 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
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-8 |
Odds Ratio | 1.1100 [1.09-1.12] |
[PMID 15752431] Association between a variation in the phosphodiesterase 4D gene and bone mineral density.
[PMID 16584842] Variants in the RAB3A gene are not associated with mental retardation in the Chinese population.
[PMID 20405052] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.