SNP Report

Basic Info
| Name |
rs41423247
dbSNP
Ensembl
|
| Location |
chr5:143399010 - 143399010(1) |
| Variant Alleles |
G/C |
| Ancestral Allele |
G |
| Minor Allele |
C |
| Minor Allele Frequence |
0.254593 |
| Functional Annotation |
downstream_gene_variant; intron_variant.
|
| Consequence to Transcript |
downstream_gene_variant(ENST00000502500, ENST00000502892, ENST00000508760, ENST00000510170, ENST00000514699); intron_variant(ENST00000231509, ENST00000343796, ENST00000394464, ENST00000394466, ENST00000415690, ENST00000424646, ENST00000503201, ENST00000504572) |
| No. of Studies |
3 (Positive: 0; Negative: 3; Trend: 0) |
| Source |
Literature |
| Overlap with SZ? |
NO
|
| Overlap with MDD? |
YES
|

SNP related studies (count: 3)

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 |
| Szczepankiewicz, A.,2011 |
X2 test:allele, P-value > 0.05;the Fisher exact test:genotype, P-value > 0.05 |
No significant association was observed. |
Negative
|