SNP Report

Basic Info
Name rs925994 dbSNP Ensembl
Location chr16:85912411 - 85912411(1)
Variant Alleles C/A
Ancestral Allele C
Minor Allele A
Minor Allele Frequence 0.102636
Functional Annotation downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000563180); intron_variant(ENST00000268638, ENST00000564056, ENST00000564617, ENST00000564803, ENST00000566369, LRG_294t1); non_coding_transcript_variant(ENST00000564056); upstream_gene_variant(ENST00000562492, ENST00000569145, ENST00000569607)
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)
IRF8 interferon regulatory factor 8 16q24.1 1(1/0/0)

SNPs in LD with rs925994 (count: 0) View in gBrowse (chr16:85912411..85912411 )

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

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