SNP Report

Basic Info

Name	rs762364 dbSNP Ensembl
Location	chr21:36034551 - 36034551(1)
Variant Alleles	G/A/C
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.254593
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000332131, ENST00000399212, ENST00000399215); downstream_gene_variant(ENST00000469482); non_coding_transcript_exon_variant(ENST00000481477, ENST00000487297); non_coding_transcript_variant(ENST00000481477, ENST00000487297)
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)
SETD4	SET domain containing 4	21q22.13	1(1/0/0)

SNPs in LD with rs762364 (count: 0) View in gBrowse (chr21:36034551..36034551 )

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

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