rs3733403
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs3733403(C;G) |
Make rs3733403(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 186265981 |
Gene | F11 |
is a | snp |
is | mentioned by |
dbSNP | rs3733403 |
dbSNP (classic) | rs3733403 |
ClinGen | rs3733403 |
ebi | rs3733403 |
HLI | rs3733403 |
Exac | rs3733403 |
Gnomad | rs3733403 |
Varsome | rs3733403 |
LitVar | rs3733403 |
Map | rs3733403 |
PheGenI | rs3733403 |
Biobank | rs3733403 |
1000 genomes | rs3733403 |
hgdp | rs3733403 |
ensembl | rs3733403 |
geneview | rs3733403 |
scholar | rs3733403 |
rs3733403 | |
pharmgkb | rs3733403 |
gwascentral | rs3733403 |
openSNP | rs3733403 |
23andMe | rs3733403 |
SNPshot | rs3733403 |
SNPdbe | rs3733403 |
MSV3d | rs3733403 |
GWAS Ctlg | rs3733403 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 24086496] Genetic variants of coagulation factor XI show association with ischemic stroke up to 70 years of age
ClinVar | |
---|---|
Risk | rs3733403(G;G) |
Alt | rs3733403(G;G) |
Reference | Rs3733403(C;C) |
Significance | Non-pathogenic |
Disease | Hereditary factor XI deficiency disease |
Variation | info |
Gene | F11 |
CLNDBN | Hereditary factor XI deficiency disease |
Reversed | 0 |
HGVS | NC_000004.11:g.187187135C>G |
CLNSRC | |
CLNACC | RCV000294092.1, |