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Variant (rsID / SNP)

rs587780636

ATM

rs587780636 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATM. Location: chromosome 11, position 108,192,151. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ATMConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:108192151
Cytoband
11q22.3
HGVS
NM_000051.4(ATM):c.6572+4T>C
Allele change
Silent

Associated conditions / phenotypes

Ataxia-telangiectasia syndrome|Hereditary cancer-predisposing syndrome

Public references

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