Variant (rsID / SNP)

rs864622416

rs864622416 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATM. Location: chromosome 11, position 108,198,406. Clinical significance in the table: Pathogenic.

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Reference-table entries

ATMPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 11:108198406
Cytoband: 11q22.3
HGVS: NM_000051.4(ATM):c.7010_7011del (p.Cys2337fs)

Associated conditions / phenotypes

Ataxia-telangiectasia syndrome|Hereditary cancer-predisposing syndrome|Familial cancer of breast

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.