rs1930095
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1930095(A;A) |
Make rs1930095(A;G) |
Make rs1930095(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 108592638 |
is a | snp |
is | mentioned by |
dbSNP | rs1930095 |
dbSNP (classic) | rs1930095 |
ClinGen | rs1930095 |
ebi | rs1930095 |
HLI | rs1930095 |
Exac | rs1930095 |
Gnomad | rs1930095 |
Varsome | rs1930095 |
LitVar | rs1930095 |
Map | rs1930095 |
PheGenI | rs1930095 |
Biobank | rs1930095 |
1000 genomes | rs1930095 |
hgdp | rs1930095 |
ensembl | rs1930095 |
geneview | rs1930095 |
scholar | rs1930095 |
rs1930095 | |
pharmgkb | rs1930095 |
gwascentral | rs1930095 |
openSNP | rs1930095 |
23andMe | rs1930095 |
SNPshot | rs1930095 |
SNPdbe | rs1930095 |
MSV3d | rs1930095 |
GWAS Ctlg | rs1930095 |
GMAF | 0.4178 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20613766] Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms