Variant (rsID / SNP)

rs7294

rs7294 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VKORC1. Location: chromosome 16, position 31,102,321. Clinical significance in the table: drug response.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

VKORC1Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 16:31102321
Cytoband: 16p11.2
HGVS: NM_024006.6(VKORC1):c.*134G>A
Allele change: Silent

Associated conditions / phenotypes

warfarin response - Dosage|Vitamin K-dependent clotting factors, combined deficiency of, type 2

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.