SNP Report

Basic Info

Name	rs6972599 dbSNP Ensembl
Location	chr7:15665230 - 15665230(1)
Variant Alleles	G/T
Ancestral Allele	T
Minor Allele	G
Minor Allele Frequence	0.179313
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000262041); upstream_gene_variant(ENST00000451240)
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 rs6972599 (count: 0) View in gBrowse (chr7:15665230..15665230 )

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

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