SNP Report

Basic Info
| Name |
rs2073831
dbSNP
Ensembl
|
| Location |
chr13:76924565 - 76924565(1) |
| Variant Alleles |
C/T |
| Ancestral Allele |
C |
| Minor Allele |
T |
| Minor Allele Frequence |
0.307508 |
| Functional Annotation |
upstream_gene_variant.
|
| Consequence to Transcript |
upstream_gene_variant(ENST00000426582) |
| No. of Studies |
2 (Positive: 0; Negative: 1; Trend: 1) |
| Source |
Literature |
| Overlap with SZ? |
YES
|
| Overlap with MDD? |
NO
|

SNP related studies (count: 2)

SNP related genes (count: 2)

Overlap with SZ from cross-disorder studies (count: 1)
| Reference |
Statistical Result |
Description |
Result Category |
| Lim C.H., 2014 |
All ethnicities: OR=1.07, 95%CI =0.90-1.28, P-value=0.445; Malay: OR=0.68, 95%CI =0.49-0.95, P-value=0.025; Chinese: OR=1.35, 95%CI =1.04-1.74, P-value=0.024; Indian: OR=1.18, 95%CI =0.81-1.70, P-value=0.387 |
KCTD12 rs2073831 was significantly associated with SZ in Malays and Chinese (P= 0.024 and 0.025, respectively). |
Positive |

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