SNP Report

Basic Info
| Name |
rs2076137
dbSNP
Ensembl
|
| Location |
chr22:50077337 - 50077337(1) |
| Variant Alleles |
C/T |
| Ancestral Allele |
C |
| Minor Allele |
T |
| Minor Allele Frequence |
0.152556 |
| Functional Annotation |
intron_variant; upstream_gene_variant.
|
| Consequence to Transcript |
intron_variant(ENST00000311597, ENST00000395876, ENST00000442311); upstream_gene_variant(ENST00000470008, ENST00000483836) |
| No. of Studies |
2 (Positive: 0; Negative: 2; Trend: 0) |
| Source |
Literature |
| Overlap with SZ? |
YES
|
| Overlap with MDD? |
NO
|

SNP related studies (count: 2)

SNP related genes (count: 1)

Overlap with SZ from cross-disorder studies (count: 2)
| Reference |
Statistical Result |
Description |
Result Category |
| Selch, S., 2007 |
chi-square tests, P-value > 0.05 |
No association with the combined patient sample, SCZ or type A or type B schizophrenia was found. |
Negative |
| Verma, R.,2005(b) |
Case-control association:for SCZ, Fisher exact test, allele P-value = 0.03; chi-square test, genotype P-value(additive)=0.02, P-value(dominant)=0.01, P-value(recessive)>0.05 ;Family-Based Association:for SCZ, TDT, P-value > 0.05 |
Significant association was observed in case-control association analysis. |
Positive |

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