rs2592551

Orientation

minus

Stabilized

minus

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

Make rs2592551(C;T)

Make rs2592551(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

85553008

Gene

GGCX

is a	snp
is	mentioned by
dbSNP	rs2592551
dbSNP (classic)	rs2592551
ClinGen	rs2592551
ebi	rs2592551
HLI	rs2592551
Exac	rs2592551
Gnomad	rs2592551
Varsome	rs2592551
LitVar	rs2592551
Map	rs2592551
PheGenI	rs2592551
Biobank	rs2592551
1000 genomes	rs2592551
hgdp	rs2592551
ensembl	rs2592551
geneview	rs2592551
scholar	rs2592551
google	rs2592551
pharmgkb	rs2592551
gwascentral	rs2592551
openSNP	rs2592551
23andMe	rs2592551
SNPshot	rs2592551
SNPdbe	rs2592551
MSV3d	rs2592551
GWAS Ctlg	rs2592551

GMAF

0.3246

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 24148610] Association of GGCX gene polymorphism with warfarin dose in atrial fibrillation population in Xinjiang

ClinVar
Risk	rs2592551(T;T)
Alt	rs2592551(T;T)
Reference	Rs2592551(C;C)
Significance	Non-pathogenic
Disease	Vitamin K-Dependent Clotting Factors
Variation	info
Gene	GGCX
CLNDBN	Vitamin K-Dependent Clotting Factors
Reversed	1
HGVS	NC_000002.11:g.85780131G>A
CLNSRC
CLNACC	RCV000261373.1,