rs10203853
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10203853(A;A) |
Make rs10203853(A;T) |
Make rs10203853(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 233778772 |
Gene | MROH2A |
is a | snp |
is | mentioned by |
dbSNP | rs10203853 |
dbSNP (classic) | rs10203853 |
ClinGen | rs10203853 |
ebi | rs10203853 |
HLI | rs10203853 |
Exac | rs10203853 |
Gnomad | rs10203853 |
Varsome | rs10203853 |
LitVar | rs10203853 |
Map | rs10203853 |
PheGenI | rs10203853 |
Biobank | rs10203853 |
1000 genomes | rs10203853 |
hgdp | rs10203853 |
ensembl | rs10203853 |
geneview | rs10203853 |
scholar | rs10203853 |
rs10203853 | |
pharmgkb | rs10203853 |
gwascentral | rs10203853 |
openSNP | rs10203853 |
23andMe | rs10203853 |
SNPshot | rs10203853 |
SNPdbe | rs10203853 |
MSV3d | rs10203853 |
GWAS Ctlg | rs10203853 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 24822274] The effect of UGT1A and UGT2B polymorphisms on colorectal cancer risk: haplotype associations and gene–environment interactions