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rs11677416

From SNPedia

Orientationplus
Stabilizedplus
Make rs11677416(C;C)
Make rs11677416(C;T)
Make rs11677416(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position112771663
is asnp
is mentioned by
dbSNPrs11677416
ebirs11677416
HLIrs11677416
Exacrs11677416
Varsomers11677416
Maprs11677416
PheGenIrs11677416
hapmaprs11677416
1000 genomesrs11677416
hgdprs11677416
ensemblrs11677416
gopubmedrs11677416
geneviewrs11677416
scholarrs11677416
googlers11677416
pharmgkbrs11677416
gwascentralrs11677416
openSNPrs11677416
23andMers11677416
23andMe allrs11677416
SNP Nexus

SNPshotrs11677416
SNPdbers11677416
MSV3drs11677416
GWAS Ctlgrs11677416
GMAF0.2029
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21107309OA-icon.png]
Trait
Title Genome-Wide Pharmacogenomic Study of Neurocognition As an Indicator of Antipsychotic Treatment Response in Schizophrenia
Risk Allele
P-val 7E-7
Odds Ratio None None