SNP Report

Basic Info

Name	rs13090011 dbSNP Ensembl
Location	chr3:51694557 - 51694557(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.303714
Functional Annotation	intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000341333, ENST00000395057, ENST00000415259, ENST00000416589, ENST00000444233, ENST00000457573, ENST00000457927, ENST00000463857, ENST00000489026, ENST00000493444, ENST00000611400, ENST00000614067); non_coding_transcript_exon_variant(ENST00000364725); non_coding_transcript_variant(ENST00000364725, ENST00000463857, ENST00000489026, ENST00000493444)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
RNA5SP132	RNA, 5S ribosomal pseudogene 132	3p21.2	Mapped by LD-proxy
TEX264	testis expressed 264	3p21	Mapped by Literature SNP

SNPs in LD with rs13090011 (count: 0) View in gBrowse (chr3:51694557..51694557 )

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

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