SNP Report

Basic Info

Name	rs2835250 dbSNP Ensembl
Location	chr21:36046909 - 36046909(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.264577
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000442559); intron_variant(ENST00000332131, ENST00000399201, ENST00000399205, ENST00000399207, ENST00000399208, ENST00000399212, ENST00000399215, ENST00000424303, ENST00000429161, ENST00000446166, ENST00000481477, ENST00000485865); non_coding_transcript_variant(ENST00000481477, ENST00000485865); upstream_gene_variant(ENST00000408914, ENST00000469482, ENST00000487297)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
SETD4	SET domain containing 4	21q22.13	1(1/0/0)
RIMKLBP1	ribosomal modification protein rimK-like family member B pseudogene 1	21q22.12	Mapped by Literature SNP

SNPs in LD with rs2835250 (count: 0) View in gBrowse (chr21:36046909..36046909 )

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

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