Variant (rsID / SNP)

rs104894539

rs104894539 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VKORC1. Location: chromosome 16, position 31,105,966. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

VKORC1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 16:31105966
Cytoband: 16p11.2
HGVS: NM_024006.6(VKORC1):c.85G>T (p.Val29Leu)
Allele change: Missense_V29L

Associated conditions / phenotypes

Warfarin 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.