rs2075789
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs2075789(A;A) |
| Make rs2075789(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31740551 |
| Gene | LOC105375020, MSH5, MSH5-SAPCD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2075789 |
| dbSNP (classic) | rs2075789 |
| ClinGen | rs2075789 |
| ebi | rs2075789 |
| HLI | rs2075789 |
| Exac | rs2075789 |
| Gnomad | rs2075789 |
| Varsome | rs2075789 |
| LitVar | rs2075789 |
| Map | rs2075789 |
| PheGenI | rs2075789 |
| Biobank | rs2075789 |
| 1000 genomes | rs2075789 |
| hgdp | rs2075789 |
| ensembl | rs2075789 |
| geneview | rs2075789 |
| scholar | rs2075789 |
| rs2075789 | |
| pharmgkb | rs2075789 |
| gwascentral | rs2075789 |
| openSNP | rs2075789 |
| 23andMe | rs2075789 |
| SNPshot | rs2075789 |
| SNPdbe | rs2075789 |
| MSV3d | rs2075789 |
| GWAS Ctlg | rs2075789 |
| GMAF | 0.1212 |
| 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 17409188] Role for Msh5 in the regulation of Ig class switch recombination.
[PMID 26027715] Correlation between polymorphisms in DNA mismatch repair genes and the risk of primary hepatocellular carcinoma for the Han population in northern China
| ClinVar | |
|---|---|
| Risk | rs2075789(A;A) |
| Alt | rs2075789(A;A) |
| Reference | Rs2075789(G;G) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | MSH5-SAPCD1 MSH5 |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000006.11:g.31708328C>T |
| CLNSRC | |
| CLNACC | RCV000455959.1, |
