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rs61742245

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61742245(A;A)
Make rs61742245(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position31094624
GeneVKORC1
is asnp
is mentioned by
dbSNPrs61742245
ebirs61742245
HLIrs61742245
Exacrs61742245
Varsomers61742245
Maprs61742245
PheGenIrs61742245
hapmaprs61742245
1000 genomesrs61742245
hgdprs61742245
ensemblrs61742245
gopubmedrs61742245
geneviewrs61742245
scholarrs61742245
googlers61742245
pharmgkbrs61742245
gwascentralrs61742245
openSNPrs61742245
23andMers61742245
23andMe allrs61742245
SNP Nexus

SNPshotrs61742245
SNPdbers61742245
MSV3drs61742245
GWAS Ctlgrs61742245
Max Magnitude0
OMIM608547
Desc
Variant0007
Relatedalso
ClinVar
Risk rs61742245(A;A)
Alt rs61742245(A;A)
Reference rs61742245(C;C)
Significance Drug-response
Disease Warfarin response warfarin response - Dosage
Variation info
Gene VKORC1
CLNDBN Warfarin response warfarin response - Dosage
Reversed 0
HGVS NC_000016.9:g.31105945C>A
CLNSRC OMIM Allelic Variant PharmGKB Clinical Annotation PharmGKB
CLNACC RCV000002296.4, RCV000211202.1,


GET Evidence
VKORC1-D36Y
aa_change Asp36Tyr
aa_change_short D36Y
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.000843644
summary