Variant (rsID / SNP)

rs2740574

rs2740574 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP3A4. Location: chromosome 7, position 99,382,096. Clinical significance in the table: Benign.

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Reference-table entries

CYP3A4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:99382096
Cytoband: 7q22.1
HGVS: NM_017460.5(CYP3A4):c.-392G>A

Associated conditions / phenotypes

Cyp3a4-v|CYP3A4 PROMOTER POLYMORPHISM

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.