SNP Report

Basic Info

Name	rs10415622 dbSNP Ensembl
Location	chr19:2739698 - 2739698(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.460463
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000269740, ENST00000455372, ENST00000545664, ENST00000586572, ENST00000589363, ENST00000590875); non_coding_transcript_variant(ENST00000590875); upstream_gene_variant(ENST00000589166)
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 rs10415622 (count: 0) View in gBrowse (chr19:2739698..2739698 )

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

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