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rs3213422

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs3213422(A;C)
Make rs3213422(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position72008783
GeneDHODH
is asnp
is mentioned by
dbSNPrs3213422
ebirs3213422
HLIrs3213422
Exacrs3213422
Varsomers3213422
Maprs3213422
PheGenIrs3213422
hapmaprs3213422
1000 genomesrs3213422
hgdprs3213422
ensemblrs3213422
gopubmedrs3213422
geneviewrs3213422
scholarrs3213422
googlers3213422
pharmgkbrs3213422
gwascentralrs3213422
openSNPrs3213422
23andMers3213422
23andMe allrs3213422
SNP Nexus

SNPshotrs3213422
SNPdbers3213422
MSV3drs3213422
GWAS Ctlgrs3213422
GMAF0.4302
Max Magnitude0
? (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.



GET Evidence
DHODH-K7Q
aa_change Lys7Gln
aa_change_short K7Q
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.542392
summary



ClinVar
Risk rs3213422(C;C)
Alt rs3213422(C;C)
Reference Rs3213422(A;A)
Significance Other
Disease not specified
Variation info
Gene DHODH
CLNDBN not specified
Reversed 0
HGVS NC_000016.9:g.72042682A>C
CLNSRC UniProtKB (protein)
CLNACC RCV000116875.3,