SNP Report

Basic Info

Name	rs2284015 dbSNP Ensembl
Location	chr22:36700528 - 36700528(1)
Variant Alleles	C/G
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.295527
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000300105); upstream_gene_variant(ENST00000430281)
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)
CACNG2	calcium channel, voltage-dependent, gamma subunit 2	22q13.1	3(3/0/0)

SNPs in LD with rs2284015 (count: 0) View in gBrowse (chr22:36700528..36700528 )

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

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