rs6590109
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6590109(A;A) |
Make rs6590109(A;G) |
Make rs6590109(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 124889152 |
Gene | ROBO4 |
is a | snp |
is | mentioned by |
dbSNP | rs6590109 |
dbSNP (classic) | rs6590109 |
ClinGen | rs6590109 |
ebi | rs6590109 |
HLI | rs6590109 |
Exac | rs6590109 |
Gnomad | rs6590109 |
Varsome | rs6590109 |
LitVar | rs6590109 |
Map | rs6590109 |
PheGenI | rs6590109 |
Biobank | rs6590109 |
1000 genomes | rs6590109 |
hgdp | rs6590109 |
ensembl | rs6590109 |
geneview | rs6590109 |
scholar | rs6590109 |
rs6590109 | |
pharmgkb | rs6590109 |
gwascentral | rs6590109 |
openSNP | rs6590109 |
23andMe | rs6590109 |
SNPshot | rs6590109 |
SNPdbe | rs6590109 |
MSV3d | rs6590109 |
GWAS Ctlg | rs6590109 |
GMAF | 0.3792 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
rs6590109 has been reported to be a SNP potentially associated with increased risk for autism [PMID 18270976]