rs983332
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs983332(A;A) |
Make rs983332(A;C) |
Make rs983332(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 87666697 |
is a | snp |
is | mentioned by |
dbSNP | rs983332 |
dbSNP (classic) | rs983332 |
ClinGen | rs983332 |
ebi | rs983332 |
HLI | rs983332 |
Exac | rs983332 |
Gnomad | rs983332 |
Varsome | rs983332 |
LitVar | rs983332 |
Map | rs983332 |
PheGenI | rs983332 |
Biobank | rs983332 |
1000 genomes | rs983332 |
hgdp | rs983332 |
ensembl | rs983332 |
geneview | rs983332 |
scholar | rs983332 |
rs983332 | |
pharmgkb | rs983332 |
gwascentral | rs983332 |
openSNP | rs983332 |
23andMe | rs983332 |
SNPshot | rs983332 |
SNPdbe | rs983332 |
MSV3d | rs983332 |
GWAS Ctlg | rs983332 |
GMAF | 0.2493 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs983332 |
PubMedID | [PMID 18615156] |
Condition | Treatment response to TNF antagonists |
Gene | LMO4 |
Risk Allele | A |
pValue | 5.00E-006 |
OR | NA |
95% CI |
[PMID 20369022] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.
[PMID 20423481] Lack of replication of genetic predictors for the rheumatoid arthritis response to anti-TNF treatments: a prospective case-only study.