Variant (rsID / SNP)

rs377260382

rs377260382 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD50, IL5. Location: chromosome 5, position 131,893,019. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

RAD50Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 5:131893019
Cytoband: 5q31.1
HGVS: NM_005732.4(RAD50):c.3G>A (p.Met1Ile)
Allele change: Missense_M1I

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Nijmegen breakage syndrome-like disorder

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.