BDgene

SNP Report

Basic Info
Name rs4668331 dbSNP Ensembl
Location chr2:170849737 - 170849737(1)
Variant Alleles A/T
Ancestral Allele A
Minor Allele T
Minor Allele Frequence 0.221446
Functional Annotation downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000462739); intron_variant(ENST00000358196, ENST00000414527, ENST00000488724, ENST00000493875, ENST00000625689); NMD_transcript_variant(ENST00000414527, ENST00000493875); non_coding_transcript_variant(ENST00000488724); upstream_gene_variant(ENST00000478562)
No. of Studies 1 (Positive: 0; Negative: 1; Trend: 0)
Source Literature
Overlap with SZ? YES
Overlap with MDD? NO

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result Category
Lundorf, M. D.,2005 A/T Fisher's exact test: for BPAD, in Danish sample set, P-value...... Fisher's exact test: for BPAD, in Danish sample set, P-value(allele)=0.13, P-value(genotype)=0.14; in Scottish sample set, P-value(allele)=0.56, P-value(genotype)=0.61 More... No significant association was observed. No significant association was observed. Negative

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
GAD1 glutamate decarboxylase 1 (brain, 67kDa) 2q31 2(1/1/0)

SNPs in LD with rs4668331 (count: 10) View in gBrowse (chr2:170833210..170858623 )
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.

Literature-origin SNPs (count: 0)

LD-proxies (count: 10)


Overlap with SZ from cross-disorder studies (count: 1)
Reference Statistical Result Description Result Category
Lundorf, M. D.,2005 Fisher's exact test:for SZ, in Scottish sample set, P-value(allele)=1, P-value(genotype)=0.92 No significant association was observed. Negative

Overlap with MDD from cross-disorder studies (count: 0)