SNP Report

Basic Info

Name	rs4687599 dbSNP Ensembl
Location	chr3:51673987 - 51673987(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.179513
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000341333, ENST00000395057, ENST00000412249, ENST00000415259, ENST00000416589, ENST00000419358, ENST00000425781, ENST00000444233, ENST00000457573, ENST00000457927, ENST00000489026, ENST00000493444, ENST00000611400, ENST00000614067); non_coding_transcript_variant(ENST00000489026, ENST00000493444); upstream_gene_variant(ENST00000483429)
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)
TEX264	testis expressed 264	3p21	Mapped by Literature SNP

SNPs in LD with rs4687599 (count: 0) View in gBrowse (chr3:51673987..51673987 )

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

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