chr14:90863357:C>A Detail (hg19)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr14:90,863,357-90,863,357 |
| hg38 | chr14:90,397,013-90,397,013 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 |
|---|---|---|---|---|---|
| 0.002 | Degenerative polyarthritis | Our data implied that the -16TT (rs12885713) CALM1 core promoter genotype is not... | BeFree | 18452398 | Detail |
| <0.001 | Adolescent idiopathic scoliosis | The susceptibility of PUMC type II (double curve) AIS and lumbar curve might be ... | BeFree | 22009783 | Detail |
| <0.001 | Dissecting aneurysm of the thoracic aorta | The susceptibility of PUMC type II (double curve) AIS and lumbar curve might be ... | BeFree | 22009783 | Detail |
| 0.157 | Degenerative polyarthritis | Our data implied that the -16TT (rs12885713) CALM1 core promoter genotype is not... | BeFree | 18452398 | Detail |
| <0.001 | Dissecting aneurysm of the thoracic aorta | The current study indicates that: (i) there are statistical differences between ... | BeFree | 22009847 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| Our data implied that the -16TT (rs12885713) CALM1 core promoter genotype is not a risk factor for O... | DisGeNET | Detail |
| The susceptibility of PUMC type II (double curve) AIS and lumbar curve might be related to CALM1 rs1... | DisGeNET | Detail |
| The susceptibility of PUMC type II (double curve) AIS and lumbar curve might be related to CALM1 rs1... | DisGeNET | Detail |
| Our data implied that the -16TT (rs12885713) CALM1 core promoter genotype is not a risk factor for O... | DisGeNET | Detail |
| The current study indicates that: (i) there are statistical differences between patients with double... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs12885713 dbSNP
- Genome
- hg19
- Position
- chr14:90,863,357-90,863,357
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- A
Genome browser