chr10:96829529:A>C Detail (hg19)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr10:96,829,529-96,829,529 |
| hg38 | chr10:95,069,772-95,069,772 View the variant detail on this assembly version. |
HGVS
[No Data.]
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:[No Data.] |
| ToMMo:0.331 | |
| NCBN:[No Data.] | |
| NCBN(Hondo):[No Data.] | |
| NCBN(Ryukyu):[No Data.] | |
| East asia | ExAC:[No Data.] |
Prediction
ClinVar
| Clinical Significance | |
| Review star | [No Data.] |
| 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 |
|---|---|---|---|---|---|
| <0.001 | Ischemic stroke | CYP2C8 rs17110453 and EPHX2 rs751141 two-locus interaction increases susceptibil... | BeFree | 25839935 | Detail |
| 0.004 | Ischemic stroke | CYP2C8 rs17110453 and EPHX2 rs751141 two-locus interaction increases susceptibil... | BeFree | 25839935 | Detail |
| 0.002 | Ischemic Cerebrovascular Accident | CYP2C8 rs17110453 and EPHX2 rs751141 two-locus interaction increases susceptibil... | BeFree | 25839935 | Detail |
| <0.001 | Ischemic Cerebrovascular Accident | CYP2C8 rs17110453 and EPHX2 rs751141 two-locus interaction increases susceptibil... | BeFree | 25839935 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| CYP2C8 rs17110453 and EPHX2 rs751141 two-locus interaction increases susceptibility to ischemic stro... | DisGeNET | Detail |
| CYP2C8 rs17110453 and EPHX2 rs751141 two-locus interaction increases susceptibility to ischemic stro... | DisGeNET | Detail |
| CYP2C8 rs17110453 and EPHX2 rs751141 two-locus interaction increases susceptibility to ischemic stro... | DisGeNET | Detail |
| CYP2C8 rs17110453 and EPHX2 rs751141 two-locus interaction increases susceptibility to ischemic stro... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs17110453 dbSNP
- Genome
- hg19
- Position
- chr10:96,829,529-96,829,529
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- C
- ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- PASS
- Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- rs17110453
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.3308
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 5544
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
Genome browser