Variant (rsID / SNP)

rs61752081

rs61752081 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BCL6, LOC100131635. Location: chromosome 3, position 187,447,701. The table records no clinical significance for this variant.

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Reference-table entries

BCL6Not classified

Variant type: single nucleotide variant
Chromosome / position: 3:187447701
Cytoband: 3q27.3
HGVS: NM_001706.5(BCL6):c.492G>T (p.Glu164Asp)
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.