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rs16887244

From SNPedia

Orientationplus
Stabilizedplus
Make rs16887244(A;A)
Make rs16887244(A;G)
Make rs16887244(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position38173827
GeneLSM1
is asnp
is mentioned by
dbSNPrs16887244
dbSNP (old)rs16887244
ClinGenrs16887244
ebirs16887244
HLIrs16887244
Exacrs16887244
Gnomadrs16887244
Varsomers16887244
Maprs16887244
PheGenIrs16887244
Biobankrs16887244
1000 genomesrs16887244
hgdprs16887244
ensemblrs16887244
gopubmedrs16887244
geneviewrs16887244
scholarrs16887244
googlers16887244
pharmgkbrs16887244
gwascentralrs16887244
openSNPrs16887244
23andMers16887244
23andMe allrs16887244
SNP Nexus

SNPshotrs16887244
SNPdbers16887244
MSV3drs16887244
GWAS Ctlgrs16887244
GMAF0.2466
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22037555OA-icon.png]
Trait
Title Common variants on 8p12 and 1q24.2 confer risk of schizophrenia.
Risk Allele
P-val 1E-10
Odds Ratio 1.1900 None