SNP Report

Basic Info

Name	rs6741692 dbSNP Ensembl
Location	chr2:115546355 - 115546355(1)
Variant Alleles	C/G
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.464657
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000310323, ENST00000393146, ENST00000393147, ENST00000409163, ENST00000410059, ENST00000429914, ENST00000461250, ENST00000488208); NMD_transcript_variant(ENST00000429914); non_coding_transcript_variant(ENST00000461250, 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)=0.00000465, P-...... Non-weighted test under H0: P-value(additive)=0.00000465, P-value(dominant)=0.0000401, P-value(recessive)=0.00136; weighted test under H'0: P-value(additive)=0.0000748, P-value(dominant)=0.000139, P-value(recessive)=0.00456; logistic regression: P-value(additive)=0.00000585, P-value(dominant)=0.00005, P-value(recessive)=0.00147 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 rs6741692 (count: 0) View in gBrowse (chr2:115546355..115546355 )

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

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