SNP Report

Basic Info

Name	rs873122 dbSNP Ensembl
Location	chr15:92158790 - 92158790(1)
Variant Alleles	G/C
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.266773
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000555769, ENST00000557683); intron_variant(ENST00000318445, ENST00000424469, ENST00000555210, ENST00000555513, ENST00000555549, ENST00000555892, ENST00000561674); NMD_transcript_variant(ENST00000555210, ENST00000555892); non_coding_transcript_variant(ENST00000555513, ENST00000555549, ENST00000561674); upstream_gene_variant(ENST00000564072)
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)
SLCO3A1	solute carrier organic anion transporter family, member 3A1	15q26	2(1/1/0)

SNPs in LD with rs873122 (count: 0) View in gBrowse (chr15:92158790..92158790 )

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

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