Have questions? Visit https://www.reddit.com/r/SNPedia

rs778371

From SNPedia

Orientationminus
Stabilizedminus
Make rs778371(C;C)
Make rs778371(C;T)
Make rs778371(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position232878399
GeneNGEF
is asnp
is mentioned by
dbSNPrs778371
ebirs778371
HLIrs778371
Exacrs778371
Varsomers778371
Maprs778371
PheGenIrs778371
hapmaprs778371
1000 genomesrs778371
hgdprs778371
ensemblrs778371
gopubmedrs778371
geneviewrs778371
scholarrs778371
googlers778371
pharmgkbrs778371
gwascentralrs778371
openSNPrs778371
23andMers778371
23andMe allrs778371
SNP Nexus

SNPshotrs778371
SNPdbers778371
MSV3drs778371
GWAS Ctlgrs778371
Max Magnitude
GWAS snp
PMID [PMID 23974872OA-icon.png]
Trait Schizophrenia
Title Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
Risk Allele G
P-val 2E-8
Odds Ratio 1.09 [1.06-1.12]