Variant (rsID / SNP)

rs2588809

rs2588809 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51B. Location: chromosome 14, position 68,660,428. Clinical significance in the table: Benign.

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Reference-table entries

RAD51BBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:68660428
Cytoband: 14q24.1
HGVS: NM_133510.4(RAD51B):c.757-98173T>C
Allele change: Silent

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.