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rs2233375

From SNPedia

Orientationplus
Stabilizedplus
Make rs2233375(C;C)
Make rs2233375(C;T)
Make rs2233375(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position233031788
GeneNEU2
is asnp
is mentioned by
dbSNPrs2233375
ebirs2233375
HLIrs2233375
Exacrs2233375
Varsomers2233375
Maprs2233375
PheGenIrs2233375
hapmaprs2233375
1000 genomesrs2233375
hgdprs2233375
ensemblrs2233375
gopubmedrs2233375
geneviewrs2233375
scholarrs2233375
googlers2233375
pharmgkbrs2233375
gwascentralrs2233375
openSNPrs2233375
23andMers2233375
23andMe allrs2233375
SNP Nexus

SNPshotrs2233375
SNPdbers2233375
MSV3drs2233375
GWAS Ctlgrs2233375
Max Magnitude
? (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