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rs983332

From SNPedia

Orientationminus
Stabilizedminus
Make rs983332(A;A)
Make rs983332(A;C)
Make rs983332(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position87666697
is asnp
is mentioned by
dbSNPrs983332
ebirs983332
HLIrs983332
Exacrs983332
Varsomers983332
Maprs983332
PheGenIrs983332
hapmaprs983332
1000 genomesrs983332
hgdprs983332
ensemblrs983332
gopubmedrs983332
geneviewrs983332
scholarrs983332
googlers983332
pharmgkbrs983332
gwascentralrs983332
openSNPrs983332
23andMers983332
23andMe allrs983332
SNP Nexus

SNPshotrs983332
SNPdbers983332
MSV3drs983332
GWAS Ctlgrs983332
GMAF0.2493
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS
SNP rs983332
PubMedID [PMID 18615156OA-icon.png]
Condition Treatment response to TNF antagonists
Gene LMO4
Risk Allele A
pValue 5.00E-006
OR NA
95% CI




[PMID 20369022OA-icon.png] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.


[PMID 20423481OA-icon.png] Lack of replication of genetic predictors for the rheumatoid arthritis response to anti-TNF treatments: a prospective case-only study.


GET Evidence
rs983332
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.222222
summary