SNP Report

Basic Info
Name rs426922 dbSNP Ensembl
Location chrCHR_HSCHR6_MHC_COX_CTG1:28534411 - 28534411(1)
Variant Alleles C/T
Ancestral Allele C
Minor Allele T
Minor Allele Frequence 0.0686901
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000412168); downstream_gene_variant(ENST00000469384, ENST00000483784); non_coding_transcript_exon_variant(ENST00000442674); non_coding_transcript_variant(ENST00000442674, ENST00000550775, ENST00000551639)
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)
GPX5 glutathione peroxidase 5 6p22.1 Mapped by LD-proxy

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

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