chr1:67260421:T>C Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr1:67,726,104-67,726,104 View the variant detail on this assembly version. |
| hg38 | chr1:67,260,421-67,260,421 |
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 |
|---|---|---|---|---|---|
| 0.371 | Crohn Disease | Genome-wide association study for Crohn's disease in the Quebec Founder Populati... | GWASCAT | 17804789 | Detail |
Annotation
Genome browser