Variant (rsID / SNP)

rs11717703

rs11717703 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATR. Location: chromosome 3, position 142,171,595. Clinical significance in the table: Likely benign.

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Reference-table entries

ATRLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:142171595
Cytoband: 3q23
HGVS: NM_001184.4(ATR):c.7761+375C>T
Allele change: Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing 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.