SNP Report

Basic Info

Name	rs17281921 dbSNP Ensembl
Location	chr7:103465449 - 103465449(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.110024
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000422488); non_coding_transcript_variant(ENST00000422488)
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
Goes, F. S., 2010		G	TDT test: P-value = 0.030 OR=1.30[1.02-1.64] for all samples...... TDT test: P-value = 0.030 OR=1.30[1.02-1.64] for all samples, P-value = 0.22 OR=1.14[0.89-1.64] for females, P-value = 0.052 OR=1.42[0.99-2.08] for males. More...	nominal significant, but not significant after empirical cor...... nominal significant, but not significant after empirical correction for testing of multiple markers. More...	Positive

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
RELN	reelin	7q22	3(1/2/0)

SNPs in LD with rs17281921 (count: 0) View in gBrowse (chr7:103465449..103465449 )

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

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