Variant (rsID / SNP)

rs114216685

rs114216685 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD54B. Location: chromosome 8, position 95,403,868. Clinical significance in the table: Benign.

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Reference-table entries

RAD54BBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 8:95403868
Cytoband: 8q22.1
HGVS: NM_012415.3(RAD54B):c.1778A>G (p.Asn593Ser)
Allele change: Missense_N409S

Associated conditions / phenotypes

Non-Hodgkin lymphoma

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.