rs169713
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs169713(C;C) |
Make rs169713(C;T) |
Make rs169713(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 11920284 |
is a | snp |
is | mentioned by |
dbSNP | rs169713 |
dbSNP (classic) | rs169713 |
ClinGen | rs169713 |
ebi | rs169713 |
HLI | rs169713 |
Exac | rs169713 |
Gnomad | rs169713 |
Varsome | rs169713 |
LitVar | rs169713 |
Map | rs169713 |
PheGenI | rs169713 |
Biobank | rs169713 |
1000 genomes | rs169713 |
hgdp | rs169713 |
ensembl | rs169713 |
geneview | rs169713 |
scholar | rs169713 |
rs169713 | |
pharmgkb | rs169713 |
gwascentral | rs169713 |
openSNP | rs169713 |
23andMe | rs169713 |
SNPshot | rs169713 |
SNPdbe | rs169713 |
MSV3d | rs169713 |
GWAS Ctlg | rs169713 |
GMAF | 0.287 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20226436] A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1