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Variant (rsID / SNP)

rs3218699

ATM

rs3218699 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATM. Location: chromosome 11, position 108,196,259. 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
11:108196259
Cytoband
11q22.3
HGVS
NM_000051.4(ATM):c.6795C>T (p.Phe2265_Lys2266=)
Allele change
Synonymous_F2265F

Associated conditions / phenotypes

Ataxia-telangiectasia syndrome|Hereditary cancer-predisposing syndrome|Malignant tumor of breast

Public references

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