SNP Report

Basic Info
Name rs1812671 dbSNP Ensembl
Location chr10:67973425 - 67973425(1)
Variant Alleles T/C
Ancestral Allele T
Minor Allele C
Minor Allele Frequence 0.105431
Functional Annotation intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000277817, ENST00000373700, ENST00000395198, ENST00000412272, ENST00000427635, ENST00000460168, ENST00000473533); NMD_transcript_variant(ENST00000427635, ENST00000473533); non_coding_transcript_variant(ENST00000460168)
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 rs1812671 (count: 0) View in gBrowse (chr10:67973425..67973425 )

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

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