rs28756991
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs28756991(A;A) |
| Make rs28756991(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 14 |
| Position | 75047266 |
| Gene | MLH3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs28756991 |
| dbSNP (classic) | rs28756991 |
| ClinGen | rs28756991 |
| ebi | rs28756991 |
| HLI | rs28756991 |
| Exac | rs28756991 |
| Gnomad | rs28756991 |
| Varsome | rs28756991 |
| LitVar | rs28756991 |
| Map | rs28756991 |
| PheGenI | rs28756991 |
| Biobank | rs28756991 |
| 1000 genomes | rs28756991 |
| hgdp | rs28756991 |
| ensembl | rs28756991 |
| geneview | rs28756991 |
| scholar | rs28756991 |
| rs28756991 | |
| pharmgkb | rs28756991 |
| gwascentral | rs28756991 |
| openSNP | rs28756991 |
| 23andMe | rs28756991 |
| SNPshot | rs28756991 |
| SNPdbe | rs28756991 |
| MSV3d | rs28756991 |
| GWAS Ctlg | rs28756991 |
| GMAF | 0.0225 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22623965
] The cumulative effects of polymorphisms in the DNA mismatch repair genes and tobacco smoking in oesophageal cancer risk
| ClinVar | |
|---|---|
| Risk | rs28756991(A;A) |
| Alt | rs28756991(A;A) |
| Reference | Rs28756991(G;G) |
| Significance | Probable-non-pathogenic |
| Disease | Lynch syndrome MLH3-Related Lynch Syndrome |
| Variation | info |
| Gene | MLH3 |
| CLNDBN | Lynch syndrome MLH3-Related Lynch Syndrome |
| Reversed | 1 |
| HGVS | NC_000014.8:g.75513969C>T |
| CLNSRC | |
| CLNACC | RCV000350967.1, RCV000474910.1, |
