Variant (rsID / SNP)
rs3092857
rs3092857 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATM. Location: chromosome 11, position 108,143,299. Clinical significance in the table: Benign.
Reference-table entries
ATMBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:108143299
- Cytoband
- 11q22.3
- HGVS
- NM_000051.4(ATM):c.3118A>G (p.Met1040Val)
- Allele change
- Missense_M1040V
Associated conditions / phenotypes
B-cell non-Hodgkin lymphoma|Hereditary cancer-predisposing syndrome|Ataxia-telangiectasia syndrome|Breast and/or ovarian cancer|Hereditary breast ovarian cancer syndrome|Familial cancer of breast
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.