rs1354492
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1354492(A;A) |
Make rs1354492(A;G) |
Make rs1354492(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 33410403 |
Gene | ASIC2 |
is a | snp |
is | mentioned by |
dbSNP | rs1354492 |
dbSNP (classic) | rs1354492 |
ClinGen | rs1354492 |
ebi | rs1354492 |
HLI | rs1354492 |
Exac | rs1354492 |
Gnomad | rs1354492 |
Varsome | rs1354492 |
LitVar | rs1354492 |
Map | rs1354492 |
PheGenI | rs1354492 |
Biobank | rs1354492 |
1000 genomes | rs1354492 |
hgdp | rs1354492 |
ensembl | rs1354492 |
geneview | rs1354492 |
scholar | rs1354492 |
rs1354492 | |
pharmgkb | rs1354492 |
gwascentral | rs1354492 |
openSNP | rs1354492 |
23andMe | rs1354492 |
SNPshot | rs1354492 |
SNPdbe | rs1354492 |
MSV3d | rs1354492 |
GWAS Ctlg | rs1354492 |
GMAF | 0.3985 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21810271![]() |
Trait | |
Title | Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels. |
Risk Allele | A |
P-val | 0.000002 |
Odds Ratio | 0.1600 [0.10-0.22] IU/dL increase |