rs527589
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs527589(A;G) |
Make rs527589(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 77443594 |
Gene | PAK1 |
is a | snp |
is | mentioned by |
dbSNP | rs527589 |
dbSNP (classic) | rs527589 |
ClinGen | rs527589 |
ebi | rs527589 |
HLI | rs527589 |
Exac | rs527589 |
Gnomad | rs527589 |
Varsome | rs527589 |
LitVar | rs527589 |
Map | rs527589 |
PheGenI | rs527589 |
Biobank | rs527589 |
1000 genomes | rs527589 |
hgdp | rs527589 |
ensembl | rs527589 |
geneview | rs527589 |
scholar | rs527589 |
rs527589 | |
pharmgkb | rs527589 |
gwascentral | rs527589 |
openSNP | rs527589 |
23andMe | rs527589 |
SNPshot | rs527589 |
SNPdbe | rs527589 |
MSV3d | rs527589 |
GWAS Ctlg | rs527589 |
GMAF | 0.06152 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22419666] |
Trait | |
Title | Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts. |
Risk Allele | |
P-val | 0.000003 |
Odds Ratio | 1.7500 None |