SNP Report

Basic Info

Name	rs664631 dbSNP Ensembl
Location	chr7:64307784 - 64307784(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.190695
Functional Annotation	intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000493036); non_coding_transcript_exon_variant(ENST00000465343); non_coding_transcript_variant(ENST00000465343, ENST00000493036); upstream_gene_variant(ENST00000438373, ENST00000492322, ENST00000606716)
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 rs664631 (count: 0) View in gBrowse (chr7:64307784..64307784 )

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

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