SNP Report

Basic Info

Name	rs4733312 dbSNP Ensembl
Location	chr8:32253401 - 32253401(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.28774
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000517967, ENST00000518104, ENST00000519301, ENST00000520407, ENST00000523320, ENST00000523534, ENST00000631040); non_coding_transcript_variant(ENST00000517967, ENST00000523320); upstream_gene_variant(ENST00000363376)
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)
NRG1	neuregulin 1	8p12	15(10/5/0)
RNA5SP263	RNA, 5S ribosomal pseudogene 263	8p12	Mapped by LD-proxy

SNPs in LD with rs4733312 (count: 0) View in gBrowse (chr8:32253401..32253401 )

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

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