SNP Report

Basic Info

Name	rs4916567 dbSNP Ensembl
Location	chr3:196872451 - 196872451(1)
Variant Alleles	T/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.491613
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000323460, ENST00000419026, ENST00000445299)
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)
SENP5	SUMO1/sentrin specific peptidase 5	3q29	Mapped by Literature SNP

SNPs in LD with rs4916567 (count: 0) View in gBrowse (chr3:196872451..196872451 )

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

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