rs2233375
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2233375(C;C) |
Make rs2233375(C;T) |
Make rs2233375(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 233031788 |
Gene | NEU2 |
is a | snp |
is | mentioned by |
dbSNP | rs2233375 |
dbSNP (classic) | rs2233375 |
ClinGen | rs2233375 |
ebi | rs2233375 |
HLI | rs2233375 |
Exac | rs2233375 |
Gnomad | rs2233375 |
Varsome | rs2233375 |
LitVar | rs2233375 |
Map | rs2233375 |
PheGenI | rs2233375 |
Biobank | rs2233375 |
1000 genomes | rs2233375 |
hgdp | rs2233375 |
ensembl | rs2233375 |
geneview | rs2233375 |
scholar | rs2233375 |
rs2233375 | |
pharmgkb | rs2233375 |
gwascentral | rs2233375 |
openSNP | rs2233375 |
23andMe | rs2233375 |
SNPshot | rs2233375 |
SNPdbe | rs2233375 |
MSV3d | rs2233375 |
GWAS Ctlg | rs2233375 |
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 | 4E-6 |
Odds Ratio | 3.63 [NR] unit increase |