SNP Report

Basic Info

Name	rs11080122 dbSNP Ensembl
Location	chr17:30220317 - 30220317(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.176118
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000261707, ENST00000394821, ENST00000401766)
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)
SLC6A4	solute carrier family 6 (neurotransmitter transporter), member 4	17q11.2	44(18/26/0)

SNPs in LD with rs11080122 (count: 0) View in gBrowse (chr17:30220317..30220317 )

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

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