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)