rs8176592
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs8176592(C;C) |
Make rs8176592(C;T) |
Make rs8176592(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 187467965 |
Gene | LOC105373786, TFPI |
is a | snp |
is | mentioned by |
dbSNP | rs8176592 |
dbSNP (classic) | rs8176592 |
ClinGen | rs8176592 |
ebi | rs8176592 |
HLI | rs8176592 |
Exac | rs8176592 |
Gnomad | rs8176592 |
Varsome | rs8176592 |
LitVar | rs8176592 |
Map | rs8176592 |
PheGenI | rs8176592 |
Biobank | rs8176592 |
1000 genomes | rs8176592 |
hgdp | rs8176592 |
ensembl | rs8176592 |
geneview | rs8176592 |
scholar | rs8176592 |
rs8176592 | |
pharmgkb | rs8176592 |
gwascentral | rs8176592 |
openSNP | rs8176592 |
23andMe | rs8176592 |
SNPshot | rs8176592 |
SNPdbe | rs8176592 |
MSV3d | rs8176592 |
GWAS Ctlg | rs8176592 |
GMAF | 0.2865 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23954867] The association of idiopathic recurrent pregnancy loss with polymorphisms in haemostasis-related genes