Variant (rsID / SNP)

rs3215983

rs3215983 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP4B1. Location: chromosome 1, position 47,280,747. Clinical significance in the table: Benign.

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Reference-table entries

CYP4B1Benign

Clinical significance (as recorded): Benign
Variant type: Deletion
Chromosome / position: 1:47280747
Cytoband: 1p33
HGVS: NM_001099772.2(CYP4B1):c.884_885del (p.Asp295fs)

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.