SNP Report

Basic Info

Name	rs10180987 dbSNP Ensembl
Location	chr2:115365856 - 115365856(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.309904
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); NMD_transcript_variant(ENST00000429914); non_coding_transcript_variant(ENST00000461250, ENST00000486885)
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
Gonzalez, S., 2014			Test for linkage:Â LOD=1.29,Â P-value=0.114;Â Test for assoc...... Test for linkage:Â LOD=1.29,Â P-value=0.114;Â Test for association:Â LOD=0.27,Â P-value=0.27;Â Test for other linked variants:Â LOD=0.99,Â P-value=0.102 More...	No significant associations were observed. No significant associations were observed.	Negative

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 rs10180987 (count: 0) View in gBrowse (chr2:115365856..115365856 )

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

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