SNP Report

Basic Info

Name	rs590890 dbSNP Ensembl
Location	chr7:64312752 - 64312752(1)
Variant Alleles	T/G
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.0625
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000465343, ENST00000492322, ENST00000606716); intron_variant(ENST00000438373, ENST00000493036); non_coding_transcript_variant(ENST00000493036); upstream_gene_variant(ENST00000355095, ENST00000423484, ENST00000488621)
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)
ZNF736	zinc finger protein 736	7q11.21	Mapped by Literature SNP

SNPs in LD with rs590890 (count: 0) View in gBrowse (chr7:64312752..64312752 )

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

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