SNP Report

Basic Info

Name	rs2099166 dbSNP Ensembl
Location	chr8:27467674 - 27467674(1)
Variant Alleles	G/T
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.238818
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000518712, ENST00000520208, ENST00000520650, ENST00000521921, ENST00000524096, ENST00000637361); intron_variant(ENST00000240132, ENST00000407991, ENST00000520933, ENST00000522008, ENST00000523695, ENST00000637241); NMD_transcript_variant(ENST00000523695, ENST00000637241); non_coding_transcript_variant(ENST00000522008); upstream_gene_variant(ENST00000520600)
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)
CHRNA2	cholinergic receptor, nicotinic, alpha 2 (neuronal)	8p21	3(0/3/0)

SNPs in LD with rs2099166 (count: 0) View in gBrowse (chr8:27467674..27467674 )

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

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