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rs6138150

From SNPedia

Orientationplus
Stabilizedplus
Make rs6138150(C;C)
Make rs6138150(C;T)
Make rs6138150(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position23866372
is asnp
is mentioned by
dbSNPrs6138150
ebirs6138150
HLIrs6138150
Exacrs6138150
Varsomers6138150
Maprs6138150
PheGenIrs6138150
hapmaprs6138150
1000 genomesrs6138150
hgdprs6138150
ensemblrs6138150
gopubmedrs6138150
geneviewrs6138150
scholarrs6138150
googlers6138150
pharmgkbrs6138150
gwascentralrs6138150
openSNPrs6138150
23andMers6138150
23andMe allrs6138150
SNP Nexus

SNPshotrs6138150
SNPdbers6138150
MSV3drs6138150
GWAS Ctlgrs6138150
GMAF0.2172
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18615156OA-icon.png]
Trait Treatment response to TNF antagonists
Title Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis
Risk Allele T
P-val 0.0000030000000000000001
Odds Ratio NR NR



[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
rs6138150
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.129032
summary