Variant (rsID / SNP)

rs373489637

rs373489637 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2B6. Location: chromosome 19, position 41,512,873. Clinical significance in the table: drug response.

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Reference-table entries

CYP2B6Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 19:41512873
Cytoband: 19q13.2
HGVS: NM_000767.5(CYP2B6):c.548T>G (p.Val183Gly)
Allele change: Missense_V183G

Associated conditions / phenotypes

Efavirenz response

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.