SNP Report

Basic Info

Name	rs2007211 dbSNP Ensembl
Location	chr11:111859227 - 111859227(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.326278
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000398006, ENST00000530851, ENST00000531154, ENST00000612489, ENST00000613181, ENST00000614444, ENST00000616540, ENST00000618252, ENST00000619129, ENST00000622211); NMD_transcript_variant(ENST00000612489, ENST00000613181, ENST00000618252, ENST00000619129); non_coding_transcript_variant(ENST00000530851); upstream_gene_variant(ENST00000527714)
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 rs2007211 (count: 0) View in gBrowse (chr11:111859227..111859227 )

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

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