rs267608073
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;AAG) | 5 | Variant of uncertain significance; possible Lynch syndrome mutation |
| (AAG;AAG) | 0 | common/normal |
| Make rs267608073(-;-) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 2 |
| Position | 47801023 |
| Gene | MSH6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs267608073 |
| dbSNP (classic) | rs267608073 |
| ClinGen | rs267608073 |
| ebi | rs267608073 |
| HLI | rs267608073 |
| Exac | rs267608073 |
| Gnomad | rs267608073 |
| Varsome | rs267608073 |
| LitVar | rs267608073 |
| Map | rs267608073 |
| PheGenI | rs267608073 |
| Biobank | rs267608073 |
| 1000 genomes | rs267608073 |
| hgdp | rs267608073 |
| ensembl | rs267608073 |
| geneview | rs267608073 |
| scholar | rs267608073 |
| rs267608073 | |
| pharmgkb | rs267608073 |
| gwascentral | rs267608073 |
| openSNP | rs267608073 |
| 23andMe | rs267608073 |
| SNPshot | rs267608073 |
| SNPdbe | rs267608073 |
| MSV3d | rs267608073 |
| GWAS Ctlg | rs267608073 |
| Max Magnitude | 5 |
c.3040_3042delAAG (p.Lys1014del); also reported in literature as 1013delCTT, c.3037_3039delAAG, and p.Lys1013del.
23andMe name: i5037885
