Variant (rsID / SNP)

rs876659350

rs876659350 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATM. Location: chromosome 11, position 108,204,695. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

ATMLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: Deletion
Chromosome / position: 11:108204695
Cytoband: 11q22.3
HGVS: NM_000051.4(ATM):c.8010+1del

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Ataxia-telangiectasia syndrome

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.