SNP Report

Basic Info
Name |
rs895682
dbSNP
Ensembl
|
Location |
chr11:13323685 - 13323685(1) |
Variant Alleles |
T/C |
Ancestral Allele |
C |
Minor Allele |
T |
Minor Allele Frequence |
0.0139776 |
Functional Annotation |
intron_variant; non_coding_transcript_variant.
|
Consequence to Transcript |
intron_variant(ENST00000389707, ENST00000401424, ENST00000403290, ENST00000403510, ENST00000480685, ENST00000482049, ENST00000527998, ENST00000529050, ENST00000529388, ENST00000529825, ENST00000530357, ENST00000531665, ENST00000533520, ENST00000534544); non_coding_transcript_variant(ENST00000480685) |
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: 1)

Overlap with SZ from cross-disorder studies (count: 1)
Reference |
Statistical Result |
Description |
Result Category |
Mansour, H. A., 2006 |
TDT P-value = 0.697, Trends test=0.846 for Pittsburgh SZ/SZA |
|
Negative |

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