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Variant (rsID / SNP)

rs61742245

VKORC1

rs61742245 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VKORC1. Location: chromosome 16, position 31,105,945. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

VKORC1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
16:31105945
Cytoband
16p11.2
HGVS
NM_024006.6(VKORC1):c.106G>T (p.Asp36Tyr)
Allele change
Missense_D36Y

Associated conditions / phenotypes

Warfarin response|Vitamin K-dependent clotting factors, combined deficiency of, type 2|Thrombus

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.