rs10929302
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10929302(A;A) |
Make rs10929302(A;G) |
Make rs10929302(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 233757136 |
Gene | LOC100286922, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9 |
is a | snp |
is | mentioned by |
dbSNP | rs10929302 |
dbSNP (classic) | rs10929302 |
ClinGen | rs10929302 |
ebi | rs10929302 |
HLI | rs10929302 |
Exac | rs10929302 |
Gnomad | rs10929302 |
Varsome | rs10929302 |
LitVar | rs10929302 |
Map | rs10929302 |
PheGenI | rs10929302 |
Biobank | rs10929302 |
1000 genomes | rs10929302 |
hgdp | rs10929302 |
ensembl | rs10929302 |
geneview | rs10929302 |
scholar | rs10929302 |
rs10929302 | |
pharmgkb | rs10929302 |
gwascentral | rs10929302 |
openSNP | rs10929302 |
23andMe | rs10929302 |
SNPshot | rs10929302 |
SNPdbe | rs10929302 |
MSV3d | rs10929302 |
GWAS Ctlg | rs10929302 |
GMAF | 0.2617 |
Max Magnitude | 0 |
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 22085899] UGT1A1 is a major locus influencing bilirubin levels in African Americans
[PMID 18992148] Low-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study.
[PMID 19482841] Serum bilirubin levels on ICU admission are associated with ARDS development and mortality in sepsis.