BDgene

Core Gene from Gene Prioritization Pathways from PBA (Pathway-based Analysis) Enriched Pathways for Core Genes Enriched Pathways for Cross-disorder Genes

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SNP Report

Basic Info

Name	rs7786884 dbSNP Ensembl
Location	chr7:15658465 - 15658465(1)
Variant Alleles	C/A
Ancestral Allele	A
Minor Allele	C
Minor Allele Frequence	0.220248
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000262041)
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)
MEOX2	mesenchyme homeobox 2	7p22.1-p21.3	1(1/0/0)

SNPs in LD with rs7786884 (count: 0) View in gBrowse (chr7:15658465..15658465 )

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

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