SNP Report

Basic Info
Name rs6013677 dbSNP Ensembl
Location chr20:38025881 - 38025881(1)
Variant Alleles G/A
Ancestral Allele A
Minor Allele G
Minor Allele Frequence 0.383387
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000373447, ENST00000373448)
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)
TTI1 TELO2 interacting protein 1 20q11.23 Mapped by LD-proxy

SNPs in LD with rs6013677 (count: 0) View in gBrowse (chr20:38025881..38025881 )

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

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