rs4681
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs4681(C;T) |
Make rs4681(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 154569680 |
Gene | FGB |
is a | snp |
is | mentioned by |
dbSNP | rs4681 |
dbSNP (classic) | rs4681 |
ClinGen | rs4681 |
ebi | rs4681 |
HLI | rs4681 |
Exac | rs4681 |
Gnomad | rs4681 |
Varsome | rs4681 |
LitVar | rs4681 |
Map | rs4681 |
PheGenI | rs4681 |
Biobank | rs4681 |
1000 genomes | rs4681 |
hgdp | rs4681 |
ensembl | rs4681 |
geneview | rs4681 |
scholar | rs4681 |
rs4681 | |
pharmgkb | rs4681 |
gwascentral | rs4681 |
openSNP | rs4681 |
23andMe | rs4681 |
SNPshot | rs4681 |
SNPdbe | rs4681 |
MSV3d | rs4681 |
GWAS Ctlg | rs4681 |
GMAF | 0.1556 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20167083] Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study
ClinVar | |
---|---|
Risk | rs4681(T;T) |
Alt | rs4681(T;T) |
Reference | Rs4681(C;C) |
Significance | Probable-non-pathogenic |
Disease | not specified Afibrinogenemia |
Variation | info |
Gene | FGB |
CLNDBN | not specified Afibrinogenemia, congenital |
Reversed | 0 |
HGVS | NC_000004.11:g.155490832C>T |
CLNSRC | |
CLNACC | RCV000247915.1, RCV000339658.1, |