SNP Report

Basic Info

Name	rs10481680 dbSNP Ensembl
Location	chr9:115257680 - 115257680(1)
Variant Alleles	A/C
Ancestral Allele	A
Minor Allele	C
Minor Allele Frequence	0.182508
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000374016); upstream_gene_variant(ENST00000444701)
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)
DEC1	deleted in esophageal cancer 1	9q32	1(1/0/0)

SNPs in LD with rs10481680 (count: 0) View in gBrowse (chr9:115257680..115257680 )

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

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