SNP Report

Basic Info

Name	rs10502148 dbSNP Ensembl
Location	chr11:111777274 - 111777274(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.358826
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000532425); intron_variant(ENST00000529841, ENST00000534218); non_coding_transcript_variant(ENST00000529841, ENST00000534218)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
ALG9	ALG9, alpha-1,2-mannosyltransferase	11q23	1(0/1/0)

SNPs in LD with rs10502148 (count: 0) View in gBrowse (chr11:111777274..111777274 )

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

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