rs1671021
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1671021(A;A) |
Make rs1671021(A;G) |
Make rs1671021(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 75569090 |
Gene | LLGL2 |
is a | snp |
is | mentioned by |
dbSNP | rs1671021 |
dbSNP (classic) | rs1671021 |
ClinGen | rs1671021 |
ebi | rs1671021 |
HLI | rs1671021 |
Exac | rs1671021 |
Gnomad | rs1671021 |
Varsome | rs1671021 |
LitVar | rs1671021 |
Map | rs1671021 |
PheGenI | rs1671021 |
Biobank | rs1671021 |
1000 genomes | rs1671021 |
hgdp | rs1671021 |
ensembl | rs1671021 |
geneview | rs1671021 |
scholar | rs1671021 |
rs1671021 | |
pharmgkb | rs1671021 |
gwascentral | rs1671021 |
openSNP | rs1671021 |
23andMe | rs1671021 |
SNPshot | rs1671021 |
SNPdbe | rs1671021 |
MSV3d | rs1671021 |
GWAS Ctlg | rs1671021 |
GMAF | 0.449 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19403135] Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study