SNP Report

Basic Info

Name	rs2000052 dbSNP Ensembl
Location	chr3:195276891 - 195276891(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.440495
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000326793); downstream_gene_variant(ENST00000419899, ENST00000472860, ENST00000618471)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
ACAP2-IT1	ACAP2 intronic transcript 1	3q29	Mapped by LD-proxy
ACAP2	ArfGAP with coiled-coil, ankyrin repeat and PH domains 2	3q29	1(0/1/0)

SNPs in LD with rs2000052 (count: 0) View in gBrowse (chr3:195276891..195276891 )

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

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