SNP Report

Basic Info
Name rs891668 dbSNP Ensembl
Location chrCHR_HSCHR3_2_CTG3:197406482 - 197406482(-1)
Variant Alleles C/T
Ancestral Allele T
Minor Allele T
Minor Allele Frequence 0.291933
Functional Annotation downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000476764); intron_variant(ENST00000358186, ENST00000392378, ENST00000392379, ENST00000431056, ENST00000432819, ENST00000441275, ENST00000445160, ENST00000446746, ENST00000468710, ENST00000492681); non_coding_transcript_variant(ENST00000468710, ENST00000492681)
No. of Studies 1 (Positive: 0; Negative: 1; Trend: 0)
Source Literature
Overlap with SZ? NO
Overlap with MDD? NO

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result Category
Schosser, A.,2011 chi-square (X2) test: genotype, X2=1.8...... chi-square (X2) test: genotype, X2=1.875, P-value = 0.392; allele, X2=1.57, P-value = 0.209 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)
BDH1 3-hydroxybutyrate dehydrogenase, type 1 3q29 2(1/1/0)

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

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