SNP Report

Basic Info
Name rs9851685 dbSNP Ensembl
Location chr3:193657175 - 193657175(1)
Variant Alleles T/C
Ancestral Allele C
Minor Allele C
Minor Allele Frequence 0.466454
Functional Annotation non_coding_transcript_exon_variant; non_coding_transcript_variant; synonymous_variant.
Consequence to Transcript non_coding_transcript_exon_variant(ENST00000482865); non_coding_transcript_variant(ENST00000482865); synonymous_variant(ENST00000361150, ENST00000361510, ENST00000361715, ENST00000361828, ENST00000361908, ENST00000392438, LRG_337t1, LRG_337t2)
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)
OPA1 optic atrophy 1 (autosomal dominant) 3q29 1(0/1/0)

SNPs in LD with rs9851685 (count: 0) View in gBrowse (chr3:193657175..193657175 )

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

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