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rs701428

From SNPedia

Orientationplus
Stabilizedplus
Make rs701428(A;A)
Make rs701428(A;G)
Make rs701428(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position20241019
GeneRTN4R
is asnp
is mentioned by
dbSNPrs701428
ebirs701428
HLIrs701428
Exacrs701428
Varsomers701428
Maprs701428
PheGenIrs701428
hapmaprs701428
1000 genomesrs701428
hgdprs701428
ensemblrs701428
gopubmedrs701428
geneviewrs701428
scholarrs701428
googlers701428
pharmgkbrs701428
gwascentralrs701428
openSNPrs701428
23andMers701428
23andMe allrs701428
SNP Nexus

SNPshotrs701428
SNPdbers701428
MSV3drs701428
GWAS Ctlgrs701428
GMAF0.4688
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 24321711OA-icon.png] White matter abnormalities in 22q11.2 deletion syndrome: Preliminary associations with the Nogo-66 receptor gene and symptoms of psychosis


[PMID 19052207OA-icon.png] Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.

GWAS snp
PMID [PMID 23251661OA-icon.png]
Trait Obesity-related traits
Title Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
Risk Allele G
P-val 2E-6
Odds Ratio .04 [NR] pg/mL increase