SNP Report

Basic Info

Name	rs2953146 dbSNP Ensembl
Location	chr2:240575835 - 240575835(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.185503
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000460884, ENST00000498042); intron_variant(ENST00000270357, ENST00000437406, ENST00000451363, ENST00000464550, ENST00000471657, ENST00000486058, ENST00000493398); non_coding_transcript_exon_variant(ENST00000481757); non_coding_transcript_variant(ENST00000464550, ENST00000471657, ENST00000481757, ENST00000486058, ENST00000493398)
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)=0.00000673, P-...... Non-weighted test under H0: P-value(additive)=0.00000673, P-value(dominant)=0.000442, P-value(recessive)=0.0000121; weighted test under H'0: P-value(additive)=0.0000342, P-value(dominant)=0.00101, P-value(recessive)=0.0000473; logistic regression: P-value(additive)=0.0000157, P-value(dominant)=0.000864, P-value(recessive)=0.0000117 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)
RNPEPL1	arginyl aminopeptidase (aminopeptidase B)-like 1	2q37.3	2(1/0/1)

SNPs in LD with rs2953146 (count: 0) View in gBrowse (chr2:240575835..240575835 )

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

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