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rs1034428

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common/normal
(C;T) 2.19x increased risk for schizophrenia in females
(T;T) 2.19x increased risk for schizophrenia in females
ReferenceGRCh38 38.1/142
ChromosomeX
Position123303197
GeneGRIA3
is asnp
is mentioned by
dbSNPrs1034428
dbSNP (classic)rs1034428
ClinGenrs1034428
ebirs1034428
HLIrs1034428
Exacrs1034428
Gnomadrs1034428
Varsomers1034428
LitVarrs1034428
Maprs1034428
PheGenIrs1034428
Biobankrs1034428
1000 genomesrs1034428
hgdprs1034428
ensemblrs1034428
geneviewrs1034428
scholarrs1034428
googlers1034428
pharmgkbrs1034428
gwascentralrs1034428
openSNPrs1034428
23andMers1034428
SNPshotrs1034428
SNPdbers1034428
MSV3drs1034428
GWAS Ctlgrs1034428
GMAF0.156
Max Magnitude0
? (C;C) (C;T) (T;T) 28


Female carriers of an rs1034428(T) allele (as oriented in dbSNP) have a 2.19x higher risk for schizophrenia compared to non-carriers, and a 3.28x higher risk for a non-paranoid phenotype.


This SNP is part of a specific haplotype, rs989638-rs1034428-rs2227098 G-T-G (as oriented with respect to dbSNP) with an overall ~2x higher risk in females for schizophrenia (p=0.0008). [PMID 18163426]