Have questions? Visit https://www.reddit.com/r/SNPedia

rs699664

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs699664(A;A)
Make rs699664(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position85553413
GeneGGCX
is asnp
is mentioned by
dbSNPrs699664
dbSNP (classic)rs699664
ClinGenrs699664
ebirs699664
HLIrs699664
Exacrs699664
Gnomadrs699664
Varsomers699664
LitVarrs699664
Maprs699664
PheGenIrs699664
Biobankrs699664
1000 genomesrs699664
hgdprs699664
ensemblrs699664
geneviewrs699664
scholarrs699664
googlers699664
pharmgkbrs699664
gwascentralrs699664
openSNPrs699664
23andMers699664
SNPshotrs699664
SNPdbers699664
MSV3drs699664
GWAS Ctlgrs699664
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 23941071OA-icon.png] Association of genetic polymorphisms with warfarin dose requirements in Chinese patients


[PMID 25681132] Impact of gamma-glutamyl carboxylase gene polymorphisms on warfarin dose requirement: A systematic review and meta-analysis


[PMID 26040031] [Association of allelic polymorphisms of genes matrix Gla-protein system with ischemic atherothrombotic stroke]


ClinVar
Risk rs699664(A;A)
Alt rs699664(A;A)
Reference Rs699664(G;G)
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.85780536C>T
CLNSRC
CLNACC RCV000357323.1,