rs11683503
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11683503(C;C) |
Make rs11683503(C;T) |
Make rs11683503(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 78971042 |
is a | snp |
is | mentioned by |
dbSNP | rs11683503 |
dbSNP (classic) | rs11683503 |
ClinGen | rs11683503 |
ebi | rs11683503 |
HLI | rs11683503 |
Exac | rs11683503 |
Gnomad | rs11683503 |
Varsome | rs11683503 |
LitVar | rs11683503 |
Map | rs11683503 |
PheGenI | rs11683503 |
Biobank | rs11683503 |
1000 genomes | rs11683503 |
hgdp | rs11683503 |
ensembl | rs11683503 |
geneview | rs11683503 |
scholar | rs11683503 |
rs11683503 | |
pharmgkb | rs11683503 |
gwascentral | rs11683503 |
openSNP | rs11683503 |
23andMe | rs11683503 |
SNPshot | rs11683503 |
SNPdbe | rs11683503 |
MSV3d | rs11683503 |
GWAS Ctlg | rs11683503 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | 1E-7 |
Odds Ratio | 4.41 [NR] unit increase |