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Variant (rsID / SNP)

rs778031266

ATM

rs778031266 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATM. Location: chromosome 11, position 108,186,841. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

ATMPathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
11:108186841
Cytoband
11q22.3
HGVS
NM_000051.4(ATM):c.6198+1G>A
Allele change
Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Hereditary breast ovarian cancer syndrome|Ataxia-telangiectasia syndrome|Abnormal central motor function

Public references

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