rs12230513
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12230513(A;A) |
Make rs12230513(A;G) |
Make rs12230513(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 55522996 |
Gene | OR6C64P |
is a | snp |
is | mentioned by |
dbSNP | rs12230513 |
dbSNP (classic) | rs12230513 |
ClinGen | rs12230513 |
ebi | rs12230513 |
HLI | rs12230513 |
Exac | rs12230513 |
Gnomad | rs12230513 |
Varsome | rs12230513 |
LitVar | rs12230513 |
Map | rs12230513 |
PheGenI | rs12230513 |
Biobank | rs12230513 |
1000 genomes | rs12230513 |
hgdp | rs12230513 |
ensembl | rs12230513 |
geneview | rs12230513 |
scholar | rs12230513 |
rs12230513 | |
pharmgkb | rs12230513 |
gwascentral | rs12230513 |
openSNP | rs12230513 |
23andMe | rs12230513 |
SNPshot | rs12230513 |
SNPdbe | rs12230513 |
MSV3d | rs12230513 |
GWAS Ctlg | rs12230513 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24152035] |
Trait | Contrast sensitivity |
Title | Variants in the 1q21 risk region are associated with a visual endophenotype of autism and schizophrenia. |
Risk Allele | |
P-val | 5E-6 |
Odds Ratio | 2.69 [NR] unit decrease |