SNP Report

Basic Info

Name	rs13123649 dbSNP Ensembl
Location	chr4:188108911 - 188108911(1)
Variant Alleles	A/C
Ancestral Allele	A
Minor Allele	C
Minor Allele Frequence	0.179113
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000464002); intron_variant(ENST00000394461); non_coding_transcript_variant(ENST00000394461); upstream_gene_variant(ENST00000326754, ENST00000502707, ENST00000511771, ENST00000512729)
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)
TRIML2	tripartite motif family-like 2	4q35.2	1(0/1/0)

SNPs in LD with rs13123649 (count: 0) View in gBrowse (chr4:188108911..188108911 )

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

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