SNP Report

Basic Info

Name	rs2231529 dbSNP Ensembl
Location	chr11:3672023 - 3672023(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.0854633
Functional Annotation	downstream_gene_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000324932, ENST00000355260, ENST00000359171, ENST00000429801, ENST00000469881, ENST00000482690); intron_variant(ENST00000533346); upstream_gene_variant(ENST00000250699, ENST00000493827, ENST00000526599, ENST00000534359)
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)
NUP98	nucleoporin 98kDa	11p15	Mapped by Literature SNP
CHRNA10	cholinergic receptor, nicotinic, alpha 10 (neuronal)	11p15.5	1(0/1/0)

SNPs in LD with rs2231529 (count: 0) View in gBrowse (chr11:3672023..3672023 )

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

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