SNP Report

Basic Info

Name	rs5751604 dbSNP Ensembl
Location	chr22:23184456 - 23184456(1)
Variant Alleles	A/C
Ancestral Allele	A
Minor Allele	C
Minor Allele Frequence	0.132788
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000305877, ENST00000359540, ENST00000398512, ENST00000479188); non_coding_transcript_variant(ENST00000479188); upstream_gene_variant(ENST00000412037)
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)
BCRP8	breakpoint cluster region pseudogene 8	22q11.23	Mapped by Literature SNP
BCR	breakpoint cluster region	22q11	2(1/1/0)

SNPs in LD with rs5751604 (count: 0) View in gBrowse (chr22:23184456..23184456 )

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

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