rs199539868
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs199539868(C;C) |
Make rs199539868(C;T) |
Make rs199539868(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 233772448 |
Gene | MROH2A, UGT1A1, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9 |
is a | snp |
is | mentioned by |
dbSNP | rs199539868 |
dbSNP (classic) | rs199539868 |
ClinGen | rs199539868 |
ebi | rs199539868 |
HLI | rs199539868 |
Exac | rs199539868 |
Gnomad | rs199539868 |
Varsome | rs199539868 |
LitVar | rs199539868 |
Map | rs199539868 |
PheGenI | rs199539868 |
Biobank | rs199539868 |
1000 genomes | rs199539868 |
hgdp | rs199539868 |
ensembl | rs199539868 |
geneview | rs199539868 |
scholar | rs199539868 |
rs199539868 | |
pharmgkb | rs199539868 |
gwascentral | rs199539868 |
openSNP | rs199539868 |
23andMe | rs199539868 |
SNPshot | rs199539868 |
SNPdbe | rs199539868 |
MSV3d | rs199539868 |
GWAS Ctlg | rs199539868 |
Max Magnitude | 0 |
[PMID 24856997] [Mutations in UGT1A1 gene in neonates with hyperbilirubinemia of Guangxi Heiyi Zhuang nationality]