SNP Report

Basic Info

Name	rs13047696 dbSNP Ensembl
Location	chr21:46607264 - 46607264(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.319888
Functional Annotation	upstream_gene_variant.
Consequence to Transcript	upstream_gene_variant(ENST00000291700, ENST00000367071, ENST00000397648)
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)
S100B	S100 calcium binding protein B	21q22.3	2(1/1/0)

SNPs in LD with rs13047696 (count: 0) View in gBrowse (chr21:46607264..46607264 )

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

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