SNP Report

Basic Info

Name	rs9799809 dbSNP Ensembl
Location	chr4:8587689 - 8587689(1)
Variant Alleles	A/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.207668
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000382487, ENST00000509216); intron_variant(ENST00000514302); NMD_transcript_variant(ENST00000514302); non_coding_transcript_exon_variant(ENST00000504255); non_coding_transcript_variant(ENST00000504255); upstream_gene_variant(ENST00000360986, ENST00000382480)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
CPZ	carboxypeptidase Z	4p16.1	Mapped by Literature SNP
GPR78	G protein-coupled receptor 78	4p16.1	2(2/0/0)

SNPs in LD with rs9799809 (count: 0) View in gBrowse (chr4:8587689..8587689 )

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

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