Have questions? Visit https://www.reddit.com/r/SNPedia

rs16869652

From SNPedia

Orientationplus
Stabilizedplus
Make rs16869652(A;A)
Make rs16869652(A;G)
Make rs16869652(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position33883396
is asnp
is mentioned by
dbSNPrs16869652
dbSNP (classic)rs16869652
ClinGenrs16869652
ebirs16869652
HLIrs16869652
Exacrs16869652
Gnomadrs16869652
Varsomers16869652
LitVarrs16869652
Maprs16869652
PheGenIrs16869652
Biobankrs16869652
1000 genomesrs16869652
hgdprs16869652
ensemblrs16869652
geneviewrs16869652
scholarrs16869652
googlers16869652
pharmgkbrs16869652
gwascentralrs16869652
openSNPrs16869652
23andMers16869652
23andMe allrs16869652
SNPshotrs16869652
SNPdbers16869652
MSV3drs16869652
GWAS Ctlgrs16869652
GMAF0.09458
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 22885689]
Trait Schizophrenia
Title Genome-wide association study of multiplex schizophrenia pedigrees.
Risk Allele
P-val 5E-6
Odds Ratio 1.45 [NR]