SNP Report

Basic Info
Name rs759071 dbSNP Ensembl
Location chr19:2728579 - 2728579(1)
Variant Alleles A/G
Ancestral Allele G
Minor Allele A
Minor Allele Frequence 0.464856
Functional Annotation downstream_gene_variant; intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000269740, ENST00000545664, ENST00000589166, ENST00000589363); intron_variant(ENST00000586572); non_coding_transcript_exon_variant(ENST00000567905); non_coding_transcript_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 rs759071 (count: 0) View in gBrowse (chr19:2728579..2728579 )

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

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