Variant (rsID / SNP)

rs370680798

rs370680798 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATM. Location: chromosome 11, position 108,178,642. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ATMBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:108178642
Cytoband: 11q22.3
HGVS: NM_000051.4(ATM):c.5693G>A (p.Arg1898Gln)
Allele change: Missense_R1898Q

Associated conditions / phenotypes

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

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.