SNP Report

Basic Info
Name rs11144764 dbSNP Ensembl
Location chr9:76140233 - 76140233(1)
Variant Alleles T/C
Ancestral Allele T
Minor Allele C
Minor Allele Frequence 0.285743
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000376752, ENST00000376767, ENST00000424854, ENST00000545128)
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)
PCSK5 proprotein convertase subtilisin/kexin type 5 9q21.13 1(1/0/0)

SNPs in LD with rs11144764 (count: 0) View in gBrowse (chr9:76140233..76140233 )

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

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