SNP Report

Basic Info

Name	rs5759666 dbSNP Ensembl
Location	chr22:23260155 - 23260155(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.259784
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000467969); intron_variant(ENST00000305877, ENST00000359540, ENST00000398512, ENST00000427791, ENST00000479188, ENST00000480973); non_coding_transcript_variant(ENST00000479188, ENST00000480973); upstream_gene_variant(ENST00000426721)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 3)

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
RN7SL263P	RNA, 7SL, cytoplasmic 263, pseudogene	22q11.23	Mapped by Literature SNP

SNPs in LD with rs5759666 (count: 0) View in gBrowse (chr22:23260155..23260155 )

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

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