Variant (rsID / SNP)

rs104895045

rs104895045 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD50. Location: chromosome 5, position 131,924,341. Clinical significance in the table: Benign.

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Reference-table entries

RAD50Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:131924341
Cytoband: 5q31.1
HGVS: NM_005732.4(RAD50):c.1052-38C>T
Allele change: Silent

Associated conditions / phenotypes

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.