SNP Report

Basic Info

Name	rs6560506 dbSNP Ensembl
Location	chr9:76142251 - 76142251(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.433506
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 rs6560506 (count: 0) View in gBrowse (chr9:76142251..76142251 )

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

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