rs10094872
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10094872(A;A) |
Make rs10094872(A;T) |
Make rs10094872(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 8 |
Position | 127707639 |
Gene | CASC11 |
is a | snp |
is | mentioned by |
dbSNP | rs10094872 |
dbSNP (classic) | rs10094872 |
ClinGen | rs10094872 |
ebi | rs10094872 |
HLI | rs10094872 |
Exac | rs10094872 |
Gnomad | rs10094872 |
Varsome | rs10094872 |
LitVar | rs10094872 |
Map | rs10094872 |
PheGenI | rs10094872 |
Biobank | rs10094872 |
1000 genomes | rs10094872 |
hgdp | rs10094872 |
ensembl | rs10094872 |
geneview | rs10094872 |
scholar | rs10094872 |
rs10094872 | |
pharmgkb | rs10094872 |
gwascentral | rs10094872 |
openSNP | rs10094872 |
23andMe | rs10094872 |
SNPshot | rs10094872 |
SNPdbe | rs10094872 |
MSV3d | rs10094872 |
GWAS Ctlg | rs10094872 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 24861552] |
Trait | Urinary bladder cancer |
Title | Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer. |
Risk Allele | T |
P-val | 2E-7 |
Odds Ratio | 1.26 |