SNP Report

Basic Info

Name	rs1362006 dbSNP Ensembl
Location	chr12:111304418 - 111304418(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.387979
Functional Annotation	downstream_gene_variant; intron_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000617342); intron_variant(ENST00000261726)
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)
CUX2	cut-like homeobox 2	12q24.12	3(1/2/0)

SNPs in LD with rs1362006 (count: 0) View in gBrowse (chr12:111304418..111304418 )

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

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