SNP Report

Basic Info
Name rs6058339 dbSNP Ensembl
Location chr20:35872557 - 35872557(1)
Variant Alleles C/T
Ancestral Allele T
Minor Allele C
Minor Allele Frequence 0.0265575
Functional Annotation downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000485604, ENST00000486408); intron_variant(ENST00000339089, ENST00000374000, ENST00000374012, ENST00000481202, ENST00000495338); non_coding_transcript_variant(ENST00000481202, ENST00000495338)
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)
PHF20 PHD finger protein 20 20q11.22-q11.23 1(0/1/0)

SNPs in LD with rs6058339 (count: 0) View in gBrowse (chr20:35872557..35872557 )

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

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