Variant (rsID / SNP)

rs9923231

rs9923231 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VKORC1. Location: chromosome 16, position 31,107,689. Clinical significance in the table: drug response.

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Reference-table entries

VKORC1Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 16:31107689
Cytoband: 16p11.2
HGVS: NM_024006.4(VKORC1):c.-1639G>A

Associated conditions / phenotypes

Warfarin response|phenprocoumon response - Dosage|warfarin response - Toxicity|phenprocoumon response - Toxicity

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.