SNP Report

Basic Info
Name rs11587594 dbSNP Ensembl
Location chr1:168019942 - 168019942(1)
Variant Alleles A/T
Ancestral Allele A
Minor Allele T
Minor Allele Frequence 0.170727
Functional Annotation intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000312263, ENST00000367840, ENST00000367843, ENST00000432587, ENST00000470721); NMD_transcript_variant(ENST00000470721); non_coding_transcript_exon_variant(ENST00000460432); non_coding_transcript_variant(ENST00000460432)
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)
DCAF6 DDB1 and CUL4 associated factor 6 1q23.3 1(0/1/0)

SNPs in LD with rs11587594 (count: 0) View in gBrowse (chr1:168019942..168019942 )

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

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