SNP Report

Basic Info

Name	rs747107 dbSNP Ensembl
Location	chr16:55661809 - 55661809(1)
Variant Alleles	T/A/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.195288
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 rs747107 (count: 0) View in gBrowse (chr16:55661809..55661809 )

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

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