Variant (rsID / SNP)
rs462779
rs462779 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to REV3L. Location: chromosome 6, position 111,695,887. The table records no clinical significance for this variant.
Reference-table entries
REV3LNot classified
- Variant type
- missense_variant
- Chromosome / position
- 6:111695887
- HGVS
- NM_001372078.1,c.3671C>T,p.Thr1224Ile
- Allele change
- Missense_T1224I
Associated conditions / phenotypes
Rectum Cancer|Lung Cancer|Neutropenia|Mesothelioma, Malignant|Lung Cancer Susceptibility 1|Osteogenic Sarcoma|Benign Mesothelioma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.