SNP Report

Basic Info
| Name |
rs12487591
dbSNP
Ensembl
|
| Location |
chr3:52608920 - 52608920(1) |
| Variant Alleles |
A/T |
| Ancestral Allele |
T |
| Minor Allele |
T |
| Minor Allele Frequence |
0.322484 |
| Functional Annotation |
downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
|
| Consequence to Transcript |
downstream_gene_variant(ENST00000480064); intron_variant(ENST00000296302, ENST00000337303, ENST00000356770, ENST00000394830, ENST00000409057, ENST00000409114, ENST00000409767, ENST00000410007, ENST00000412587, ENST00000423351, ENST00000446103, ENST00000462207); NMD_transcript_variant(ENST00000412587); non_coding_transcript_variant(ENST00000462207) |
| No. of Studies |
1 (Positive: 1; Negative: 0; Trend: 0) |
| Source |
Literature |
| Overlap with SZ? |
NO
|
| Overlap with MDD? |
YES
|

SNP related studies (count: 1)

SNP related genes (count: 1)

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

Overlap with MDD from cross-disorder studies (count: 1)
| Reference |
Statistical Result |
Description |
Result Category |
| Major Depressive Disorder Working Group of the Psychiatric, G. C., 2013 |
P-value=0.006943, OR=1.063 for MDD, P-value=0.00000003091, OR=1.098 for combined sample |
In the combined analysis of these 819 SNPs, 15 exceeded genome-wide significance and all were in a 248 kb interval of high LD on 3p21.9. |
Positive
|