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rs17863783

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs17863783(G;T)
Make rs17863783(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position233693631
GeneUGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs17863783
ebirs17863783
HLIrs17863783
Exacrs17863783
Varsomers17863783
Maprs17863783
PheGenIrs17863783
hapmaprs17863783
1000 genomesrs17863783
hgdprs17863783
ensemblrs17863783
gopubmedrs17863783
geneviewrs17863783
scholarrs17863783
googlers17863783
pharmgkbrs17863783
gwascentralrs17863783
openSNPrs17863783
23andMers17863783
23andMe allrs17863783
SNP Nexus

SNPshotrs17863783
SNPdbers17863783
MSV3drs17863783
GWAS Ctlgrs17863783
GMAF0.05234
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 22228101OA-icon.png] Mapping of the UGT1A locus identifies an uncommon coding variant that affects mRNA expression and protects from bladder cancer


[PMID 23441093] Validation of variants in SLC28A3 and UGT1A6 as genetic markers predictive of anthracycline-induced cardiotoxicity in children