SNP Report

Basic Info

Name	rs4964489 dbSNP Ensembl
Location	chr12:106778030 - 106778030(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.380391
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000355478, ENST00000392837, ENST00000392839, ENST00000462949, ENST00000470628, ENST00000548914, ENST00000549643, ENST00000550215, ENST00000552619); NMD_transcript_variant(ENST00000462949, ENST00000550215); non_coding_transcript_variant(ENST00000470628); upstream_gene_variant(ENST00000549203, ENST00000551505)
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 rs4964489 (count: 0) View in gBrowse (chr12:106778030..106778030 )

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

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