chr1:100719028:T>C Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr1:101,184,584-101,184,584 View the variant detail on this assembly version. |
| hg38 | chr1:100,719,028-100,719,028 |
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 |
|---|---|---|---|---|---|
| <0.001 | Graves Disease | Although there is not association between ICAM1 (G241R and K469E), VCAM1 (T-1591... | BeFree | 23242661 | Detail |
Annotation
Genome browser