rs104894542

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs104894542(G;G)

Make rs104894542(G;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

31091243

Gene	PRSS53, VKORC1

is a	snp
is	mentioned by
dbSNP	rs104894542
dbSNP (classic)	rs104894542
ClinGen	rs104894542
ebi	rs104894542
HLI	rs104894542
Exac	rs104894542
Gnomad	rs104894542
Varsome	rs104894542
LitVar	rs104894542
Map	rs104894542
PheGenI	rs104894542
Biobank	rs104894542
1000 genomes	rs104894542
hgdp	rs104894542
ensembl	rs104894542
geneview	rs104894542
scholar	rs104894542
google	rs104894542
pharmgkb	rs104894542
gwascentral	rs104894542
openSNP	rs104894542
23andMe	rs104894542
SNPshot	rs104894542
SNPdbe	rs104894542
MSV3d	rs104894542
GWAS Ctlg	rs104894542

Merged from

Rs28940305

Max Magnitude

0

OMIM	608547
Desc
Variant	0005
Related	also

ClinVar
Risk	rs104894542(G;G)
Alt	rs104894542(G;G)
Reference	Rs104894542(T;T)
Significance	Pathogenic
Disease	Warfarin response
Variation	info
Gene	VKORC1
CLNDBN	Warfarin response
Reversed	1
HGVS	NC_000016.9:g.31102564A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000002294.2,