rs10235789
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10235789(C;C) |
Make rs10235789(C;T) |
Make rs10235789(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 84027484 |
Gene | SEMA3A |
is a | snp |
is | mentioned by |
dbSNP | rs10235789 |
dbSNP (classic) | rs10235789 |
ClinGen | rs10235789 |
ebi | rs10235789 |
HLI | rs10235789 |
Exac | rs10235789 |
Gnomad | rs10235789 |
Varsome | rs10235789 |
LitVar | rs10235789 |
Map | rs10235789 |
PheGenI | rs10235789 |
Biobank | rs10235789 |
1000 genomes | rs10235789 |
hgdp | rs10235789 |
ensembl | rs10235789 |
geneview | rs10235789 |
scholar | rs10235789 |
rs10235789 | |
pharmgkb | rs10235789 |
gwascentral | rs10235789 |
openSNP | rs10235789 |
23andMe | rs10235789 |
SNPshot | rs10235789 |
SNPdbe | rs10235789 |
MSV3d | rs10235789 |
GWAS Ctlg | rs10235789 |
GMAF | 0.3154 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21835309] |
Trait | |
Title | GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development. |
Risk Allele | C |
P-val | 7E-11 |
Odds Ratio | 0.1200 [0.08-0.16] unit increase |