SNP Report

Basic Info
Name |
rs7611731
dbSNP
Ensembl
|
Location |
chr3:52658705 - 52658705(1) |
Variant Alleles |
T/C |
Ancestral Allele |
C |
Minor Allele |
C |
Minor Allele Frequence |
0.444089 |
Functional Annotation |
downstream_gene_variant; intron_variant; NMD_transcript_variant.
|
Consequence to Transcript |
downstream_gene_variant(ENST00000420148); intron_variant(ENST00000296302, ENST00000337303, ENST00000356770, ENST00000394830, ENST00000409057, ENST00000409114, ENST00000409767, ENST00000410007, ENST00000412587, ENST00000423351, ENST00000431678, ENST00000446103); NMD_transcript_variant(ENST00000412587) |
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=0.01077, OR=1.059 for MDD, P-value=0.00000004995, OR=1.096 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 3p21.15. |
Positive
|