SNP Report

Basic Info

Name	rs4451148 dbSNP Ensembl
Location	chr6:132619154 - 132619154(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.304712
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000367931); upstream_gene_variant(ENST00000275191)
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)
TAAR2	trace amine associated receptor 2	6q24	Mapped by Literature SNP

SNPs in LD with rs4451148 (count: 0) View in gBrowse (chr6:132619154..132619154 )

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

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