chr6:32718326:C>T Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr6:32,686,103-32,686,103 View the variant detail on this assembly version. |
| hg38 | chr6:32,718,326-32,718,326 |
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 |
|---|---|---|---|---|---|
| 0.043 | Lupus Erythematosus, Systemic | [We identified and then confirmed through replication two new genetic loci for S... | GAD | 18204098 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| [We identified and then confirmed through replication two new genetic loci for SLE: a promoter-regio... | DisGeNET | Detail |
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs9275659 dbSNP
- Genome
- hg38
- Position
- chr6:32,718,326-32,718,326
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
Genome browser