rs11705932
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11705932(C;C) |
| Make rs11705932(C;T) |
| Make rs11705932(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 3 |
| Position | 142100008 |
| Gene | TFDP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11705932 |
| dbSNP (classic) | rs11705932 |
| ClinGen | rs11705932 |
| ebi | rs11705932 |
| HLI | rs11705932 |
| Exac | rs11705932 |
| Gnomad | rs11705932 |
| Varsome | rs11705932 |
| LitVar | rs11705932 |
| Map | rs11705932 |
| PheGenI | rs11705932 |
| Biobank | rs11705932 |
| 1000 genomes | rs11705932 |
| hgdp | rs11705932 |
| ensembl | rs11705932 |
| geneview | rs11705932 |
| scholar | rs11705932 |
| rs11705932 | |
| pharmgkb | rs11705932 |
| gwascentral | rs11705932 |
| openSNP | rs11705932 |
| 23andMe | rs11705932 |
| SNPshot | rs11705932 |
| SNPdbe | rs11705932 |
| MSV3d | rs11705932 |
| GWAS Ctlg | rs11705932 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
A multi-stage GWAS study of 6,000+ patients with testicular cancer found this SNP (and 3 others) to be associated with slightly higher risk (OR 1.18 for risk allele C; CI: 1.09–1.28, p=1.5x10e−9) for the disease. See also the testicular cancer page for the discussion of this and the 24 other SNPs used in a polygenic risk score.[PMID 26503584
]
