SNP Report

Basic Info

Name	rs11076111 dbSNP Ensembl
Location	chr16:55660639 - 55660639(1)
Variant Alleles	G/C
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.247404
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000219833, ENST00000379906, ENST00000414754, ENST00000561820, ENST00000566163, ENST00000568529, ENST00000568655, ENST00000568943)
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)
SLC6A2	solute carrier family 6 (neurotransmitter transporter), member 2	16q12.2	2(0/2/0)

SNPs in LD with rs11076111 (count: 0) View in gBrowse (chr16:55660639..55660639 )

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

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