SNP Report

Basic Info
Name rs3758393 dbSNP Ensembl
Location chr10:68032964 - 68032964(1)
Variant Alleles T/C
Ancestral Allele T
Minor Allele C
Minor Allele Frequence 0.0988419
Functional Annotation downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000513996); intron_variant(ENST00000277817, ENST00000373700, ENST00000395198, ENST00000412272, ENST00000427635, ENST00000463478, ENST00000473533); NMD_transcript_variant(ENST00000427635, ENST00000473533); non_coding_transcript_variant(ENST00000463478)
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)
HERC4 HECT and RLD domain containing E3 ubiquitin protein ligase 4 10q21.3 Mapped by Literature SNP

SNPs in LD with rs3758393 (count: 0) View in gBrowse (chr10:68032964..68032964 )

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

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