SNP Report

Basic Info

Name	rs3840795 dbSNP Ensembl
Location	chr12:111363028 - 111363036(1)
Variant Alleles	CCCCGCCAC/-
Minor Allele Frequence	0.0
Functional Annotation	downstream_gene_variant; inframe_deletion.
Consequence to Transcript	downstream_gene_variant(ENST00000547710, ENST00000549321); inframe_deletion(ENST00000361483, ENST00000547838, ENST00000548163)
No. of Studies	1 (Positive: 1; Negative: 0; Trend: 0)
Source	Literature
Overlap with SZ?	NO
Overlap with MDD?	NO

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result Category
Glaser, B.,2005(b)	D/I		For Sample I+II, allelic association: X²=7.56, P-...... For Sample I+II, allelic association: X²=7.56, P-value = 0.005, OR(95%CI)=0.7(0.5-0.9); genotypic association: X²=7.73, P-value = 0.02. For family based study, TDT: X²=0.67, P-value < 0.2. More...	Significant association was observed in both allelic associa...... Significant association was observed in both allelic association and genotypic association, but No significant association was observed in family based study. More...	Positive

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
FAM109A	family with sequence similarity 109, member A	12q24.12	1(1/0/0)

SNPs in LD with rs3840795 (count: 0) View in gBrowse (chr12:111363028..111363036 )

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

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