SNP Report

Basic Info
Name rs12995487 dbSNP Ensembl
Location chr2:159392606 - 159392606(1)
Variant Alleles C/G
Ancestral Allele C
Minor Allele G
Minor Allele Frequence 0.230232
Functional Annotation intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000294905, ENST00000392782, ENST00000392783, ENST00000420020, ENST00000551504); non_coding_transcript_variant(ENST00000420020, ENST00000551504); upstream_gene_variant(ENST00000485917, ENST00000594921, ENST00000608714, ENST00000626302)
No. of Studies 0 (Positive: 0; Negative: 0; Trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
BAZ2B bromodomain adjacent to zinc finger domain, 2B 2q24.2 1(0/1/0)

SNPs in LD with rs12995487 (count: 0) View in gBrowse (chr2:159392606..159392606 )

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

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