rs1059060
From SNPedia
| Merged into | rs17420802 |
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs1059060(A;G) |
| Make rs1059060(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 5977709 |
| Gene | PMS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1059060 |
| dbSNP (classic) | rs1059060 |
| ClinGen | rs1059060 |
| ebi | rs1059060 |
| HLI | rs1059060 |
| Exac | rs1059060 |
| Gnomad | rs1059060 |
| Varsome | rs1059060 |
| LitVar | rs1059060 |
| Map | rs1059060 |
| PheGenI | rs1059060 |
| Biobank | rs1059060 |
| 1000 genomes | rs1059060 |
| hgdp | rs1059060 |
| ensembl | rs1059060 |
| geneview | rs1059060 |
| scholar | rs1059060 |
| rs1059060 | |
| pharmgkb | rs1059060 |
| gwascentral | rs1059060 |
| openSNP | rs1059060 |
| 23andMe | rs1059060 |
| SNPshot | rs1059060 |
| SNPdbe | rs1059060 |
| MSV3d | rs1059060 |
| GWAS Ctlg | rs1059060 |
| Status | Merged into rs17420802 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22594646
] Common variants in mismatch repair genes associated with increased risk of sperm DNA damage and male infertility[PMID 17267408] Allelic imbalance in gene expression as a guide to cis-acting regulatory single nucleotide polymorphisms in cancer cells.
[PMID 26027715] Correlation between polymorphisms in DNA mismatch repair genes and the risk of primary hepatocellular carcinoma for the Han population in northern China
