rs1133950
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs1133950(G;G) |
Make rs1133950(G;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 8 |
Position | 116771675 |
Gene | UTP23 |
is a | snp |
is | mentioned by |
dbSNP | rs1133950 |
dbSNP (classic) | rs1133950 |
ClinGen | rs1133950 |
ebi | rs1133950 |
HLI | rs1133950 |
Exac | rs1133950 |
Gnomad | rs1133950 |
Varsome | rs1133950 |
LitVar | rs1133950 |
Map | rs1133950 |
PheGenI | rs1133950 |
Biobank | rs1133950 |
1000 genomes | rs1133950 |
hgdp | rs1133950 |
ensembl | rs1133950 |
geneview | rs1133950 |
scholar | rs1133950 |
rs1133950 | |
pharmgkb | rs1133950 |
gwascentral | rs1133950 |
openSNP | rs1133950 |
23andMe | rs1133950 |
SNPshot | rs1133950 |
SNPdbe | rs1133950 |
MSV3d | rs1133950 |
GWAS Ctlg | rs1133950 |
GMAF | 0.0652 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 19471308] A genome-wide scan of 10 000 gene-centric variants and colorectal cancer risk