rs77120160
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs77120160(A;A) |
| Make rs77120160(A;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 37047500 |
| Gene | MLH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs77120160 |
| dbSNP (classic) | rs77120160 |
| ClinGen | rs77120160 |
| ebi | rs77120160 |
| HLI | rs77120160 |
| Exac | rs77120160 |
| Gnomad | rs77120160 |
| Varsome | rs77120160 |
| LitVar | rs77120160 |
| Map | rs77120160 |
| PheGenI | rs77120160 |
| Biobank | rs77120160 |
| 1000 genomes | rs77120160 |
| hgdp | rs77120160 |
| ensembl | rs77120160 |
| geneview | rs77120160 |
| scholar | rs77120160 |
| rs77120160 | |
| pharmgkb | rs77120160 |
| gwascentral | rs77120160 |
| openSNP | rs77120160 |
| 23andMe | rs77120160 |
| SNPshot | rs77120160 |
| SNPdbe | rs77120160 |
| MSV3d | rs77120160 |
| GWAS Ctlg | rs77120160 |
| GMAF | 0.00551 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs77120160(A;A) |
| Alt | rs77120160(A;A) |
| Reference | Rs77120160(T;T) |
| Significance | Other |
| Disease | Lynch syndrome not specified |
| Variation | info |
| Gene | MLH1 |
| CLNDBN | Lynch syndrome not specified |
| Reversed | 0 |
| HGVS | NC_000003.11:g.37088991T>A |
| CLNSRC | HGMD |
| CLNACC | RCV000030216.3, RCV000078418.5, |
[PMID 21056691
] Prevalence of alterations in DNA mismatch repair genes in patients with young-onset colorectal cancer.
