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rs2949006

From SNPedia

Orientationplus
Stabilizedplus
Make rs2949006(G;G)
Make rs2949006(G;T)
Make rs2949006(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position199850665
GeneFTCDNL1
is asnp
is mentioned by
dbSNPrs2949006
ebirs2949006
HLIrs2949006
Exacrs2949006
Varsomers2949006
Maprs2949006
PheGenIrs2949006
hapmaprs2949006
1000 genomesrs2949006
hgdprs2949006
ensemblrs2949006
gopubmedrs2949006
geneviewrs2949006
scholarrs2949006
googlers2949006
pharmgkbrs2949006
gwascentralrs2949006
openSNPrs2949006
23andMers2949006
23andMe allrs2949006
SNP Nexus

SNPshotrs2949006
SNPdbers2949006
MSV3drs2949006
GWAS Ctlgrs2949006
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 T
P-val 1E-8
Odds Ratio 1.10 [1.07-1.14]