SNP Report

Basic Info
Name rs13359903 dbSNP Ensembl
Location chr5:148548336 - 148548336(1)
Variant Alleles T/C
Ancestral Allele C
Minor Allele C
Minor Allele Frequence 0.261781
Functional Annotation downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000519495); intron_variant(ENST00000360693, ENST00000362016, ENST00000377888, ENST00000517929, ENST00000520514, ENST00000521124, ENST00000521530, ENST00000521735, ENST00000522588, ENST00000524063, ENST00000631296); NMD_transcript_variant(ENST00000522588, ENST00000524063); non_coding_transcript_variant(ENST00000521124)
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)
HTR4 5-hydroxytryptamine (serotonin) receptor 4, G protein-coupled 5q31-q33 2(1/1/0)

SNPs in LD with rs13359903 (count: 0) View in gBrowse (chr5:148548336..148548336 )

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

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