SNP Report

Basic Info
| Name |
rs6295
dbSNP
Ensembl
|
| Location |
chr5:63962738 - 63962738(1) |
| Variant Alleles |
C/G |
| Ancestral Allele |
G |
| Minor Allele |
C |
| Minor Allele Frequence |
0.453275 |
| Functional Annotation |
intron_variant; non_coding_transcript_variant; upstream_gene_variant.
|
| Consequence to Transcript |
intron_variant(ENST00000502882); non_coding_transcript_variant(ENST00000502882); upstream_gene_variant(ENST00000323865, ENST00000506598) |
| No. of Studies |
2 (Positive: 2; Negative: 0; Trend: 0) |
| Source |
Literature |
| Overlap with SZ? |
YES
|
| Overlap with MDD? |
YES
|

SNP related studies (count: 2)

SNP related genes (count: 1)

Overlap with SZ from cross-disorder studies (count: 1)
| Reference |
Statistical Result |
Description |
Result Category |
| Kishi, T.,2011(b) |
For SZ, chi-square tests:genotype, P-value = 0.12;allele, P-value = 0.146;meta analysis:random model:pooled OR=0.793, 95% CI=0.387-1.623, P(Z)=0.526 |
No significant association was observed. |
Negative |

Overlap with MDD from cross-disorder studies (count: 1)
| Reference |
Statistical Result |
Description |
Result Category |
| Kishi, T.,2012(a) |
Meta analysis:MDD: P (allele model) = 0.006, P (recessive model) = 0.01 |
Significant association was found. |
Positive
|