SNP Report

Basic Info

Name	rs4862858 dbSNP Ensembl
Location	chr4:188095961 - 188095961(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.14397
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000511771); intron_variant(ENST00000326754, ENST00000503141, ENST00000503475, ENST00000512729); NMD_transcript_variant(ENST00000503141, ENST00000503475)
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 rs4862858 (count: 0) View in gBrowse (chr4:188095961..188095961 )

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

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