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rs17206232

From SNPedia

Orientationplus
Stabilizedplus
Make rs17206232(A;A)
Make rs17206232(A;C)
Make rs17206232(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position65137573
is asnp
is mentioned by
dbSNPrs17206232
ebirs17206232
HLIrs17206232
Exacrs17206232
Varsomers17206232
Maprs17206232
PheGenIrs17206232
hapmaprs17206232
1000 genomesrs17206232
hgdprs17206232
ensemblrs17206232
gopubmedrs17206232
geneviewrs17206232
scholarrs17206232
googlers17206232
pharmgkbrs17206232
gwascentralrs17206232
openSNPrs17206232
23andMers17206232
23andMe allrs17206232
SNP Nexus

SNPshotrs17206232
SNPdbers17206232
MSV3drs17206232
GWAS Ctlgrs17206232
GMAF0.07897
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23212062OA-icon.png]
Trait Schizophrenia
Title Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.
Risk Allele
P-val 1E-6
Odds Ratio .14 [NR] unit increase