SNP Report

Basic Info

Name	rs6803763 dbSNP Ensembl
Location	chr3:195358213 - 195358213(1)
Variant Alleles	A/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.402556
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000326793, ENST00000480906, ENST00000481463, ENST00000618471, ENST00000635383); non_coding_transcript_variant(ENST00000480906, ENST00000481463); upstream_gene_variant(ENST00000423531)
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)
ACAP2	ArfGAP with coiled-coil, ankyrin repeat and PH domains 2	3q29	1(0/1/0)

SNPs in LD with rs6803763 (count: 0) View in gBrowse (chr3:195358213..195358213 )

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

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