SNP Report

Basic Info

Name	rs3809272 dbSNP Ensembl
Location	chr12:111362454 - 111362454(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.247005
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000361483, ENST00000547838, ENST00000548163); downstream_gene_variant(ENST00000547710, ENST00000549321)
No. of Studies	1 (Positive: 0; Negative: 1; 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)	A/G		For Sample I, allelic association: X²=0.07, P-val...... For Sample I, allelic association: X²=0.07, P-value = 0.79, OR(95%CI)=1(0.8-1.4); genotypic association: X²=0.35, P-value = 0.84 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)
FAM109A	family with sequence similarity 109, member A	12q24.12	1(1/0/0)

SNPs in LD with rs3809272 (count: 0) View in gBrowse (chr12:111362454..111362454 )

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

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