SNP Report

Basic Info

Name	rs3759310 dbSNP Ensembl
Location	chr12:106772344 - 106772344(1)
Variant Alleles	C/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.405152
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000549203, ENST00000551505); non_coding_transcript_variant(ENST00000549203, ENST00000551505); upstream_gene_variant(ENST00000355478, ENST00000392837, ENST00000392839, ENST00000462949, ENST00000470628, ENST00000548914, ENST00000549643, ENST00000550215, ENST00000552619)
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)
RIC8B	RIC8 guanine nucleotide exchange factor B	12q23.3	Mapped by LD-proxy

SNPs in LD with rs3759310 (count: 0) View in gBrowse (chr12:106772344..106772344 )

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

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