rs754716792
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (TC;TC) | 0 | common in clinvar |
| Make rs754716792(-;-) |
| Make rs754716792(-;TC) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 14 |
| Position | 75046862 |
| Gene | MLH3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs754716792 |
| dbSNP (classic) | rs754716792 |
| ClinGen | rs754716792 |
| ebi | rs754716792 |
| HLI | rs754716792 |
| Exac | rs754716792 |
| Gnomad | rs754716792 |
| Varsome | rs754716792 |
| LitVar | rs754716792 |
| Map | rs754716792 |
| PheGenI | rs754716792 |
| Biobank | rs754716792 |
| 1000 genomes | rs754716792 |
| hgdp | rs754716792 |
| ensembl | rs754716792 |
| geneview | rs754716792 |
| scholar | rs754716792 |
| rs754716792 | |
| pharmgkb | rs754716792 |
| gwascentral | rs754716792 |
| openSNP | rs754716792 |
| 23andMe | rs754716792 |
| SNPshot | rs754716792 |
| SNPdbe | rs754716792 |
| MSV3d | rs754716792 |
| GWAS Ctlg | rs754716792 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs754716792(-;-) |
| Alt | rs754716792(-;-) |
| Reference | Rs754716792(TC;TC) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | MLH3 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000014.8:g.75513565_75513566delTC |
| CLNSRC | |
| CLNACC | RCV000486748.1, |
