SNP Report

Basic Info

Name	rs1176738 dbSNP Ensembl
Location	chr11:113937373 - 113937373(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.076877
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000260191, ENST00000537778, ENST00000543092)
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)
HTR3B	5-hydroxytryptamine (serotonin) receptor 3B, ionotropic	11q23.1	2(1/1/0)

SNPs in LD with rs1176738 (count: 0) View in gBrowse (chr11:113937373..113937373 )

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

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