SNP Report

Basic Info

Name	rs10407667 dbSNP Ensembl
Location	chr19:2731529 - 2731529(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.465855
Functional Annotation	downstream_gene_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000269740, ENST00000455372, ENST00000545664, ENST00000589166, ENST00000589363); intron_variant(ENST00000586572); upstream_gene_variant(ENST00000567905)
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)
SLC39A3	solute carrier family 39 (zinc transporter), member 3	19p13.3	1(0/1/0)

SNPs in LD with rs10407667 (count: 0) View in gBrowse (chr19:2731529..2731529 )

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

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