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Rs1034428

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is asnp
is mentioned by
dbSNPrs1034428
hapmaprs1034428
hgdprs1034428
ensemblrs1034428
gopubmedrs1034428
scholarrs1034428
googlers1034428
pharmgkbrs1034428
hgvbaseg2prs1034428
medrefsnprs1034428
23andMers1034428
SNP Nexus

GeneGRIA3
ChromosomeX
Orientationminus
Position122264729
GenotypeEffect
rs1034428(C;C)2.19x increased risk for schizophrenia in females
rs1034428(C;T)2.19x increased risk for schizophrenia in females
rs1034428(T;T)normal


Genotypes Magnitude Summary
Rs1034428(C;C) 2.19x increased risk for schizophrenia in females
Rs1034428(C;T) 2.19x increased risk for schizophrenia in females
Rs1034428(T;T) normal
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]

? (C;C) (C;T) (T;T)
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