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rs115329265

From SNPedia

Merged intors1233578
Orientationplus
Stabilizedplus
Make rs115329265(A;A)
Make rs115329265(A;G)
Make rs115329265(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position28744470
is asnp
is mentioned by
dbSNPrs115329265
dbSNP (classic)rs115329265
ClinGenrs115329265
ebirs115329265
HLIrs115329265
Exacrs115329265
Gnomadrs115329265
Varsomers115329265
LitVarrs115329265
Maprs115329265
PheGenIrs115329265
Biobankrs115329265
1000 genomesrs115329265
hgdprs115329265
ensemblrs115329265
geneviewrs115329265
scholarrs115329265
googlers115329265
pharmgkbrs115329265
gwascentralrs115329265
openSNPrs115329265
23andMers115329265
SNPshotrs115329265
SNPdbers115329265
MSV3drs115329265
GWAS Ctlgrs115329265
StatusMerged into rs1233578
Max Magnitude0

A study ranked this SNP first in terms of evidence from p value for schizophrenia risk.

The A allele is reference (G allele is risk) OR=1.205(95 CI 1.168-1.244) p= 3.48e-31.