rs7925879
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7925879(A;A) |
Make rs7925879(A;G) |
Make rs7925879(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 124870795 |
Gene | ROBO3 |
is a | snp |
is | mentioned by |
dbSNP | rs7925879 |
dbSNP (classic) | rs7925879 |
ClinGen | rs7925879 |
ebi | rs7925879 |
HLI | rs7925879 |
Exac | rs7925879 |
Gnomad | rs7925879 |
Varsome | rs7925879 |
LitVar | rs7925879 |
Map | rs7925879 |
PheGenI | rs7925879 |
Biobank | rs7925879 |
1000 genomes | rs7925879 |
hgdp | rs7925879 |
ensembl | rs7925879 |
geneview | rs7925879 |
scholar | rs7925879 |
rs7925879 | |
pharmgkb | rs7925879 |
gwascentral | rs7925879 |
openSNP | rs7925879 |
23andMe | rs7925879 |
SNPshot | rs7925879 |
SNPdbe | rs7925879 |
MSV3d | rs7925879 |
GWAS Ctlg | rs7925879 |
GMAF | 0.371 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
rs7925879 has been reported to be a SNP potentially associated with increased risk for autism [PMID 18270976]
[PMID 17846999] A chromosome 11q quantitative-trait locus influences change of blood-pressure measurements over time in Mexican Americans of the San Antonio Family Heart Study.