SNP Report

Basic Info
Name |
rs1156026
dbSNP
Ensembl
|
Location |
chr13:43152209 - 43152209(1) |
Variant Alleles |
T/C |
Ancestral Allele |
T |
Minor Allele |
C |
Minor Allele Frequence |
0.467053 |
No. of Studies |
1 (Positive: 1; Negative: 0; Trend: 0) |
Source |
Literature |
Overlap with SZ? |
YES
|
Overlap with MDD? |
NO
|

SNP related studies (count: 1)

SNP related genes (count: 0)

Overlap with SZ from cross-disorder studies (count: 1)
Reference |
Statistical Result |
Description |
Result Category |
Bureau A, 2013 |
Fisher’s exact test, P-value=4.4E-06, OR (95% CI)=1.81 (1.39, 2.35), FDR=0.014 in all cases of the case-contro sample; P-value=0.012, OR (95% CI)=1.54 (1.1, 2.17) in all families of the kindred sample; P-value=8.5E-07, OR (95% CI)=1.69 (1.37, 2.08) for the combined analyses; P-value=8.8E-04, OR (95% CI)=2.03 (1.34, 3.09) in SZ families of the kindred sample; P-value=6.4E-08, OR (95% CI)=1.85 (1.48, 2.31) for the combined analyses; P-value=0.012, OR (95% CI)=1.54 (1.1, 2.17) |
An association of the T allele of rs1156026 found in the case-control sample was replicated in the kindred sample, strengthening the overall association evidence. |
Positive |

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