Variant (rsID / SNP)

rs201686625

rs201686625 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATM. Location: chromosome 11, position 108,119,654. Clinical significance in the table: Benign.

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Reference-table entries

ATMBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:108119654
Cytoband: 11q22.3
HGVS: NM_000051.4(ATM):c.1066-6T>G
Allele change: Silent

Associated conditions / phenotypes

Ataxia-telangiectasia syndrome|Hereditary cancer-predisposing syndrome|Familial cancer of breast|Malignant tumor of breast|Breast and/or ovarian cancer

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.