SNP Report

Basic Info
Name rs2694831 dbSNP Ensembl
Location chr12:79693000 - 79693000(1)
Variant Alleles G/A
Ancestral Allele G
Minor Allele A
Minor Allele Frequence 0.290535
Functional Annotation intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000551995); non_coding_transcript_variant(ENST00000551995); upstream_gene_variant(ENST00000328827, ENST00000547016, ENST00000547571, ENST00000548426, ENST00000550006, ENST00000551712, ENST00000552637)
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)
PAWR PRKC, apoptosis, WT1, regulator 12q21.2 1(0/1/0)

SNPs in LD with rs2694831 (count: 0) View in gBrowse (chr12:79693000..79693000 )

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

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