SNP Report

Basic Info

Name	rs2020942 dbSNP Ensembl
Location	chr17:30219896 - 30219896(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.254992
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000261707, ENST00000394821, ENST00000401766)
No. of Studies	2 (Positive: 0; Negative: 2; Trend: 0)
Source	Literature
Overlap with SZ?	NO
Overlap with MDD?	NO

SNP related studies (count: 2)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result Category
Alaerts, M.,2009	A/G		Allelic association P-value = 0.31; Genotypic association P-...... Allelic association P-value = 0.31; Genotypic association P-value = 0.34 More...	No significant association was observed No significant association was observed	Negative
Mansour, H. A.,2005	G/A		Pittsburgh BD1 sample: trends test for case-control analysis...... Pittsburgh BD1 sample: trends test for case-control analysis, P-value = 0.586; TDT T/NT=25/26; STEP-BD sample: trends test for case-control analysis, P-value = Pittsburgh BD1 sample: trends test for case-control analysis, P-value = 0.586; TDT T/NT=25/26 More...	No significant association was observed. No significant association was observed.	Negative

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 rs2020942 (count: 0) View in gBrowse (chr17:30219896..30219896 )

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

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