rs3213422
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs3213422(A;C) |
Make rs3213422(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 72008783 |
Gene | DHODH |
is a | snp |
is | mentioned by |
dbSNP | rs3213422 |
dbSNP (classic) | rs3213422 |
ClinGen | rs3213422 |
ebi | rs3213422 |
HLI | rs3213422 |
Exac | rs3213422 |
Gnomad | rs3213422 |
Varsome | rs3213422 |
LitVar | rs3213422 |
Map | rs3213422 |
PheGenI | rs3213422 |
Biobank | rs3213422 |
1000 genomes | rs3213422 |
hgdp | rs3213422 |
ensembl | rs3213422 |
geneview | rs3213422 |
scholar | rs3213422 |
rs3213422 | |
pharmgkb | rs3213422 |
gwascentral | rs3213422 |
openSNP | rs3213422 |
23andMe | rs3213422 |
SNPshot | rs3213422 |
SNPdbe | rs3213422 |
MSV3d | rs3213422 |
GWAS Ctlg | rs3213422 |
GMAF | 0.4302 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 19207032] The frequency of remission from rheumatoid arthritis upon leflunomide treatment was increased in rs3213422(C) allele carriers compared with patients with the A allele in a study of 147 patients.
ClinVar | |
---|---|
Risk | rs3213422(C;C) |
Alt | rs3213422(C;C) |
Reference | Rs3213422(A;A) |
Significance | Other |
Disease | not specified Miller syndrome |
Variation | info |
Gene | DHODH |
CLNDBN | not specified Miller syndrome |
Reversed | 0 |
HGVS | NC_000016.9:g.72042682A>C |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000116875.3, RCV000321810.1, |