SNP Report

Basic Info

Name	rs2149356 dbSNP Ensembl
Location	chr9:117711921 - 117711921(1)
Variant Alleles	T/G
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.478834
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000490685); intron_variant(ENST00000355622, ENST00000394487, ENST00000472304); non_coding_transcript_variant(ENST00000472304); upstream_gene_variant(ENST00000364574)
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)
RNU6-1082P	RNA, U6 small nuclear 1082, pseudogene	9q33.1	Mapped by LD-proxy
TLR4	toll-like receptor 4	9q33.1	1(1/0/0)

SNPs in LD with rs2149356 (count: 0) View in gBrowse (chr9:117711921..117711921 )

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

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