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rs9610449

From SNPedia

Orientationplus
Stabilizedplus
Make rs9610449(C;C)
Make rs9610449(C;T)
Make rs9610449(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position36215187
is asnp
is mentioned by
dbSNPrs9610449
ebirs9610449
HLIrs9610449
Exacrs9610449
Varsomers9610449
Maprs9610449
PheGenIrs9610449
hapmaprs9610449
1000 genomesrs9610449
hgdprs9610449
ensemblrs9610449
gopubmedrs9610449
geneviewrs9610449
scholarrs9610449
googlers9610449
pharmgkbrs9610449
gwascentralrs9610449
openSNPrs9610449
23andMers9610449
23andMe allrs9610449
SNP Nexus

SNPshotrs9610449
SNPdbers9610449
MSV3drs9610449
GWAS Ctlgrs9610449
GMAF0.2475
Max Magnitude
[PMID 18632255OA-icon.png] rs9610449 schizophrenia (377 families, 1161 genotyped members and 647 genotyped affected in total) rs9610449 and rs6000200 associated with risk for schizophrenia in African-Americans. In the combined (AA and EA) sample, two SNPs, rs2003813 and rs2157249