rs2075786
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2075786(C;C) |
| Make rs2075786(C;T) |
| Make rs2075786(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 1266195 |
| Gene | TERT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2075786 |
| dbSNP (classic) | rs2075786 |
| ClinGen | rs2075786 |
| ebi | rs2075786 |
| HLI | rs2075786 |
| Exac | rs2075786 |
| Gnomad | rs2075786 |
| Varsome | rs2075786 |
| LitVar | rs2075786 |
| Map | rs2075786 |
| PheGenI | rs2075786 |
| Biobank | rs2075786 |
| 1000 genomes | rs2075786 |
| hgdp | rs2075786 |
| ensembl | rs2075786 |
| geneview | rs2075786 |
| scholar | rs2075786 |
| rs2075786 | |
| pharmgkb | rs2075786 |
| gwascentral | rs2075786 |
| openSNP | rs2075786 |
| 23andMe | rs2075786 |
| SNPshot | rs2075786 |
| SNPdbe | rs2075786 |
| MSV3d | rs2075786 |
| GWAS Ctlg | rs2075786 |
| GMAF | 0.4417 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 22495810] Association of genetic variants of human telomerase with colorectal polyps and colorectal cancer risk
[PMID 19285750
] Genetic variation in telomere maintenance genes, telomere length, and lung cancer susceptibility.
[PMID 20445798] Chromosome 5p Region SNPs Are Associated with Risk of NSCLC among Women.
[PMID 22948024] Genetic variant in the telomerase gene modifies cancer risk in Lynch syndrome.
