SNP Report

Basic Info
| Name |
rs989713
dbSNP
Ensembl
|
| Location |
chr6:37681935 - 37681935(1) |
| Variant Alleles |
C/T |
| Ancestral Allele |
T |
| Minor Allele |
C |
| Minor Allele Frequence |
0.113419 |
| Functional Annotation |
intron_variant.
|
| Consequence to Transcript |
intron_variant(ENST00000434837, ENST00000505425, ENST00000515437) |
| No. of Studies |
1 (Positive: 0; Negative: 1; Trend: 0) |
| Source |
Literature |
| Overlap with SZ? |
YES
|
| Overlap with MDD? |
YES
|

SNP related studies (count: 1)

SNP related genes (count: 1)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.
Literature-origin SNPs (count: 0)
LD-proxies (count: 5)

| rs_ID |
Literature-origin SNPs with LD |
Functional Annotation |
r2[population] |
|
rs9394449
|
|
intron_variant |
1.0[CHB]; 1.0[JPT]
|
|
rs6458011
|
|
intron_variant |
0.802[CHD]; 1.0[JPT]
|
|
rs9394450
|
|
intron_variant |
0.904[CHB]; 1.0[JPT]
|
|
rs6458012
|
|
intron_variant |
1.0[JPT]
|
|
rs876796
|
|
intron_variant |
1.0[CHB]; 1.0[JPT]
|

Overlap with SZ from cross-disorder studies (count: 1)
| Reference |
Statistical Result |
Description |
Result Category |
| Li, J.,2011(a) |
Single SNP analyses:allele, P-value = 0.2801, OR[95%CI]=1.1064[0.9209, 1.3294], genotype, P-value = 0.0969 for SZ |
No significant association was observed. |
Negative |

Overlap with MDD from cross-disorder studies (count: 1)
| Reference |
Statistical Result |
Description |
Result Category |
| Li, J.,2011(a) |
Single SNP analyses:allele, P-value = 0.0748, OR[95%CI]=1.1775[0.9837, 1.4094], genotype, P-value = 0.1617 for MDD |
No significant association was observed. |
Negative
|