rs1016342
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1016342(C;C) |
| Make rs1016342(C;T) |
| Make rs1016342(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 127080210 |
| Gene | PCAT2, PRNCR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1016342 |
| dbSNP (classic) | rs1016342 |
| ClinGen | rs1016342 |
| ebi | rs1016342 |
| HLI | rs1016342 |
| Exac | rs1016342 |
| Gnomad | rs1016342 |
| Varsome | rs1016342 |
| LitVar | rs1016342 |
| Map | rs1016342 |
| PheGenI | rs1016342 |
| Biobank | rs1016342 |
| 1000 genomes | rs1016342 |
| hgdp | rs1016342 |
| ensembl | rs1016342 |
| geneview | rs1016342 |
| scholar | rs1016342 |
| rs1016342 | |
| pharmgkb | rs1016342 |
| gwascentral | rs1016342 |
| openSNP | rs1016342 |
| 23andMe | rs1016342 |
| SNPshot | rs1016342 |
| SNPdbe | rs1016342 |
| MSV3d | rs1016342 |
| GWAS Ctlg | rs1016342 |
| GMAF | 0.4614 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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[PMID 19562729
] Common variants in 8q24 are associated with risk for prostate cancer and tumor aggressiveness in men of European ancestry
