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rs2592551

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2592551(C;T)
Make rs2592551(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position85553008
GeneGGCX
is asnp
is mentioned by
dbSNPrs2592551
dbSNP (old)rs2592551
ClinGenrs2592551
ebirs2592551
HLIrs2592551
Exacrs2592551
Varsomers2592551
Maprs2592551
PheGenIrs2592551
Biobankrs2592551
1000 genomesrs2592551
hgdprs2592551
ensemblrs2592551
gopubmedrs2592551
geneviewrs2592551
scholarrs2592551
googlers2592551
pharmgkbrs2592551
gwascentralrs2592551
openSNPrs2592551
23andMers2592551
23andMe allrs2592551
SNP Nexus

SNPshotrs2592551
SNPdbers2592551
MSV3drs2592551
GWAS Ctlgrs2592551
GMAF0.3246
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 24148610OA-icon.png] 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,