Variant (rsID / SNP)

rs2108622

rs2108622 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP4F2. Location: chromosome 19, position 15,990,431. Clinical significance in the table: drug response.

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Reference-table entries

CYP4F2Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 19:15990431
Cytoband: 19p13.12
HGVS: NM_001082.5(CYP4F2):c.1297G>A (p.Val433Met)
Allele change: Missense_V433M

Associated conditions / phenotypes

acenocoumarol response - Dosage|warfarin response - Dosage

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.