SNP Report

Basic Info

Name	rs4141060 dbSNP Ensembl
Location	chr3:50262685 - 50262685(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.432907
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000266027, ENST00000313601, ENST00000421735, ENST00000422163, ENST00000440628, ENST00000441156, ENST00000446079, ENST00000451956, ENST00000453717, ENST00000490122, ENST00000491100, ENST00000492383); intron_variant(ENST00000426302, ENST00000439898); non_coding_transcript_variant(ENST00000426302, ENST00000439898); upstream_gene_variant(ENST00000618865, ENST00000621029)
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)
SEMA3B	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3B	3p21.3	Mapped by LD-proxy
GNAI2	guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 2	3p21.31	1(0/1/0)

SNPs in LD with rs4141060 (count: 0) View in gBrowse (chr3:50262685..50262685 )

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

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