SNP Report

Basic Info

Name	rs4821392 dbSNP Ensembl
Location	chr22:35294539 - 35294539(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.473043
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000216106, ENST00000418170); downstream_gene_variant(ENST00000498212, ENST00000609073); NMD_transcript_variant(ENST00000418170); upstream_gene_variant(ENST00000447733, ENST00000608674, ENST00000608749)
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)
TOM1	target of myb1 (chicken)	22q13.1	1(1/0/0)
HMGXB4	HMG box domain containing 4	22q13	1(1/0/0)

SNPs in LD with rs4821392 (count: 0) View in gBrowse (chr22:35294539..35294539 )

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

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