chr5:131993452:T>C Detail (hg19)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr5:131,993,452-131,993,452 |
| hg38 | chr5:132,657,760-132,657,760 View the variant detail on this assembly version. |
HGVS
[No Data.]
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.010 | schizophrenia | This study aimed at investigating the association between schizophrenia suscepti... | BeFree | 24065520 | Detail |
| 0.127 | schizophrenia | This study aimed at investigating the association between schizophrenia suscepti... | BeFree | 24065520 | Detail |
| 0.001 | schizophrenia | This study aimed at investigating the association between schizophrenia suscepti... | BeFree | 24065520 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| This study aimed at investigating the association between schizophrenia susceptibility and selected ... | DisGeNET | Detail |
| This study aimed at investigating the association between schizophrenia susceptibility and selected ... | DisGeNET | Detail |
| This study aimed at investigating the association between schizophrenia susceptibility and selected ... | DisGeNET | Detail |
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs2069756 dbSNP
- Genome
- hg19
- Position
- chr5:131,993,452-131,993,452
- Variant Type
- snv
- Reference Allele
- T
- Alternative Allele
- C
Genome browser