Variant (rsID / SNP)

rs371320628

rs371320628 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD50. Location: chromosome 5, position 131,927,565. Clinical significance in the table: Likely benign.

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Reference-table entries

RAD50Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 5:131927565
Cytoband: 5q31.1
HGVS: NM_005732.4(RAD50):c.1636-4A>G
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.