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rs10929302

From SNPedia

Orientationplus
Stabilizedplus
Make rs10929302(A;A)
Make rs10929302(A;G)
Make rs10929302(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position233757136
GeneUGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs10929302
ebirs10929302
HLIrs10929302
Exacrs10929302
Varsomers10929302
Maprs10929302
PheGenIrs10929302
hapmaprs10929302
1000 genomesrs10929302
hgdprs10929302
ensemblrs10929302
gopubmedrs10929302
geneviewrs10929302
scholarrs10929302
googlers10929302
pharmgkbrs10929302
gwascentralrs10929302
openSNPrs10929302
23andMers10929302
23andMe allrs10929302
SNP Nexus

SNPshotrs10929302
SNPdbers10929302
MSV3drs10929302
GWAS Ctlgrs10929302
GMAF0.2617
Max Magnitude
Clinically relevant UGT1A10 variant.
? (A;A) (A;G) (G;G) 28



[PMID 21309756] Prevalence of clinically relevant UGT1A alleles and haplotypes in African populations


[PMID 22085899OA-icon.png] UGT1A1 is a major locus influencing bilirubin levels in African Americans


[PMID 18992148OA-icon.png] Low-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study.


[PMID 19482841OA-icon.png] Serum bilirubin levels on ICU admission are associated with ARDS development and mortality in sepsis.


GET Evidence
rs10929302
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.301587
summary