Variant (rsID / SNP)

rs61730467

rs61730467 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BCL9L. Location: chromosome 11, position 118,772,160. Clinical significance in the table: Benign.

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Reference-table entries

BCL9LBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:118772160
Cytoband: 11q23.3
HGVS: NM_001378213.1(BCL9L):c.2292C>T (p.Pro764=)
Allele change: Synonymous_P764P

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.