SNP Report

Basic Info

Name	rs20572 dbSNP Ensembl
Location	chr21:36072675 - 36072675(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.1252
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; intron_variant; non_coding_transcript_variant; synonymous_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000530908); downstream_gene_variant(ENST00000399191, ENST00000415147, ENST00000439427, ENST00000466328); intron_variant(ENST00000399201, ENST00000535199); non_coding_transcript_variant(ENST00000535199); synonymous_variant(ENST00000290349)
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)
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 rs20572 (count: 0) View in gBrowse (chr21:36072675..36072675 )

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

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