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Variant (rsID / SNP)

rs8017304

RAD51B

rs8017304 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51B. Location: chromosome 14, position 68,785,077. The table records no clinical significance for this variant.

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Reference-table entries

RAD51BNot classified
Variant type
single nucleotide variant
Chromosome / position
14:68785077
Cytoband
14q24.1
HGVS
NM_133510.4(RAD51B):c.853+26380G>A
Allele change
Silent

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.