rs4675502
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4675502(A;A) |
Make rs4675502(A;G) |
Make rs4675502(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 205221447 |
Gene | PARD3B |
is a | snp |
is | mentioned by |
dbSNP | rs4675502 |
dbSNP (classic) | rs4675502 |
ClinGen | rs4675502 |
ebi | rs4675502 |
HLI | rs4675502 |
Exac | rs4675502 |
Gnomad | rs4675502 |
Varsome | rs4675502 |
LitVar | rs4675502 |
Map | rs4675502 |
PheGenI | rs4675502 |
Biobank | rs4675502 |
1000 genomes | rs4675502 |
hgdp | rs4675502 |
ensembl | rs4675502 |
geneview | rs4675502 |
scholar | rs4675502 |
rs4675502 | |
pharmgkb | rs4675502 |
gwascentral | rs4675502 |
openSNP | rs4675502 |
23andMe | rs4675502 |
SNPshot | rs4675502 |
SNPdbe | rs4675502 |
MSV3d | rs4675502 |
GWAS Ctlg | rs4675502 |
GMAF | 0.433 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22843504] |
Trait | Autism |
Title | Individual common variants exert weak effects on the risk for autism spectrum disorderspi. |
Risk Allele | |
P-val | 4E-7 |
Odds Ratio | 1.28 [1.16-1.41] |