rs1991867
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1991867(A;A) |
Make rs1991867(A;G) |
Make rs1991867(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 82485623 |
is a | snp |
is | mentioned by |
dbSNP | rs1991867 |
dbSNP (classic) | rs1991867 |
ClinGen | rs1991867 |
ebi | rs1991867 |
HLI | rs1991867 |
Exac | rs1991867 |
Gnomad | rs1991867 |
Varsome | rs1991867 |
LitVar | rs1991867 |
Map | rs1991867 |
PheGenI | rs1991867 |
Biobank | rs1991867 |
1000 genomes | rs1991867 |
hgdp | rs1991867 |
ensembl | rs1991867 |
geneview | rs1991867 |
scholar | rs1991867 |
rs1991867 | |
pharmgkb | rs1991867 |
gwascentral | rs1991867 |
openSNP | rs1991867 |
23andMe | rs1991867 |
SNPshot | rs1991867 |
SNPdbe | rs1991867 |
MSV3d | rs1991867 |
GWAS Ctlg | rs1991867 |
GMAF | 0.2185 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21502573![]() |
Trait | |
Title | Genetic predictors of fibrin D-dimer levels in healthy adults. |
Risk Allele | C |
P-val | 0.000004 |
Odds Ratio | 0.0440 [NR] % decrease |
GWAS snp | |
---|---|
PMID | [PMID 24736177![]() |
Trait | White matter microstructure (global fractional anisotropy) |
Title | Common genetic variants and gene expression associated with white matter microstructure in the human brain. |
Risk Allele | |
P-val | 2E-9 |
Odds Ratio | NR NR |