Variant (rsID / SNP)

rs8023214

rs8023214 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51B. Location: chromosome 14, position 69,117,512. The table records no clinical significance for this variant.

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Reference-table entries

RAD51BNot classified

Variant type: intron_variant
Chromosome / position: 14:69117512
HGVS: NM_001321818.2,c.1037-32142T>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.