BDgene

SNP Report

Basic Info
Name rs6970492 dbSNP Ensembl
Location chr7:15615540 - 15615540(1)
Variant Alleles T/C
Ancestral Allele C
Minor Allele T
Minor Allele Frequence 0.335863
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 rs6970492 (count: 0) View in gBrowse (chr7:15615540..15615540 )

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

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