SNP Report

Basic Info

Name	rs5759669 dbSNP Ensembl
Location	chr22:23267313 - 23267313(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.334265
Functional Annotation	downstream_gene_variant; intron_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000426721); intron_variant(ENST00000305877, ENST00000359540, ENST00000398512, ENST00000427791)
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)
BCR	breakpoint cluster region	22q11	2(1/1/0)
FBXW4P1	F-box and WD repeat domain containing 4 pseudogene 1	22q11	Mapped by Literature SNP

SNPs in LD with rs5759669 (count: 0) View in gBrowse (chr22:23267313..23267313 )

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

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