SNP Report

Basic Info

Name	rs2267361 dbSNP Ensembl
Location	chr22:36704215 - 36704215(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.465855
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000430281); non_coding_transcript_variant(ENST00000430281); upstream_gene_variant(ENST00000300105)
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 rs2267361 (count: 0) View in gBrowse (chr22:36704215..36704215 )

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

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