SNP Report

Basic Info

Name	rs11123306 dbSNP Ensembl
Location	chr2:115474205 - 115474205(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.458466
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000310323, ENST00000393146, ENST00000393147, ENST00000409163, ENST00000410059, ENST00000419287, ENST00000429914, ENST00000436732, ENST00000461250, ENST00000486885, ENST00000488208); NMD_transcript_variant(ENST00000429914); non_coding_transcript_variant(ENST00000461250, ENST00000486885, ENST00000488208)
No. of Studies	1 (Positive: 0; Negative: 0; Trend: 1)
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
Jiang, Y.,2011			Non-weighted test under H0: P-value(additive)=0.00000279, P-...... Non-weighted test under H0: P-value(additive)=0.00000279, P-value(dominant)=0.000076, P-value(recessive)=0.000224; weighted test under H'0: P-value(additive)=0.0000376, P-value(dominant)=0.000098, P-value(recessive)=0.000886; logistic regression: P-value(additive)=0.00000245, P-value(dominant)=0.0000567, P-value(recessive)=0.000275 More...	Suggestive association was found. Suggestive association was found.	Trend

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
DPP10	dipeptidyl-peptidase 10 (non-functional)	2q14.1	3(2/1/0)

SNPs in LD with rs11123306 (count: 0) View in gBrowse (chr2:115474205..115474205 )

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

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