Variant (rsID / SNP)

rs145301478

rs145301478 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATM. Location: chromosome 11, position 108,115,710. Clinical significance in the table: Likely benign.

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Reference-table entries

ATMLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:108115710
Cytoband: 11q22.3
HGVS: NM_000051.4(ATM):c.858A>G (p.Gln286=)
Allele change: Synonymous_Q286Q

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.