rs12603582
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12603582(G;G) |
Make rs12603582(G;T) |
Make rs12603582(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 47300211 |
Gene | ITGB3 |
is a | snp |
is | mentioned by |
dbSNP | rs12603582 |
dbSNP (classic) | rs12603582 |
ClinGen | rs12603582 |
ebi | rs12603582 |
HLI | rs12603582 |
Exac | rs12603582 |
Gnomad | rs12603582 |
Varsome | rs12603582 |
LitVar | rs12603582 |
Map | rs12603582 |
PheGenI | rs12603582 |
Biobank | rs12603582 |
1000 genomes | rs12603582 |
hgdp | rs12603582 |
ensembl | rs12603582 |
geneview | rs12603582 |
scholar | rs12603582 |
rs12603582 | |
pharmgkb | rs12603582 |
gwascentral | rs12603582 |
openSNP | rs12603582 |
23andMe | rs12603582 |
SNPshot | rs12603582 |
SNPdbe | rs12603582 |
MSV3d | rs12603582 |
GWAS Ctlg | rs12603582 |
GMAF | 0.1882 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 21102624] Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes