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rs3832043

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs3832043(-;-)
Make rs3832043(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position233671808
GeneUGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs3832043
ebirs3832043
HLIrs3832043
Exacrs3832043
Varsomers3832043
Maprs3832043
PheGenIrs3832043
hapmaprs3832043
1000 genomesrs3832043
hgdprs3832043
ensemblrs3832043
gopubmedrs3832043
geneviewrs3832043
scholarrs3832043
googlers3832043
pharmgkbrs3832043
gwascentralrs3832043
openSNPrs3832043
23andMers3832043
23andMe allrs3832043
SNP Nexus

SNPshotrs3832043
SNPdbers3832043
MSV3drs3832043
GWAS Ctlgrs3832043
Max Magnitude0


[PMID 17761781] Lack of association between common polymorphisms in UGT1A9 and gene expression and activity.


GET Evidence
rs3832043
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.435484
summary



ClinVar
Risk rs3832043(;)
Alt rs3832043(;)
Reference rs3832043(T;T)
Significance Drug-response
Disease SN-38 response - Other
Variation info
Gene UGT1A9 UGT1A8 UGT1A10
CLNDBN SN-38 response - Other
Reversed 0
HGVS NC_000002.11:g.234580454delT
CLNSRC PharmGKB Clinical Annotation PharmGKB
CLNACC RCV000211185.1,