SNP Report

Basic Info

Name	rs3787728 dbSNP Ensembl
Location	chr21:36071595 - 36071595(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.270168
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000363343, ENST00000415147, ENST00000439427, ENST00000466328); intron_variant(ENST00000290349, ENST00000399191, ENST00000399201, ENST00000530908, ENST00000535199); non_coding_transcript_variant(ENST00000535199)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 3)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
RNU6-992P	RNA, U6 small nuclear 992, pseudogene	21q22.12	Mapped by LD-proxy
CBR1	carbonyl reductase 1	21q22.1	Mapped by LD-proxy
SETD4	SET domain containing 4	21q22.13	1(1/0/0)

SNPs in LD with rs3787728 (count: 0) View in gBrowse (chr21:36071595..36071595 )

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

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