rs699664
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs699664(A;A) |
Make rs699664(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 85553413 |
Gene | GGCX |
is a | snp |
is | mentioned by |
dbSNP | rs699664 |
dbSNP (classic) | rs699664 |
ClinGen | rs699664 |
ebi | rs699664 |
HLI | rs699664 |
Exac | rs699664 |
Gnomad | rs699664 |
Varsome | rs699664 |
LitVar | rs699664 |
Map | rs699664 |
PheGenI | rs699664 |
Biobank | rs699664 |
1000 genomes | rs699664 |
hgdp | rs699664 |
ensembl | rs699664 |
geneview | rs699664 |
scholar | rs699664 |
rs699664 | |
pharmgkb | rs699664 |
gwascentral | rs699664 |
openSNP | rs699664 |
23andMe | rs699664 |
SNPshot | rs699664 |
SNPdbe | rs699664 |
MSV3d | rs699664 |
GWAS Ctlg | rs699664 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23941071] 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, |