chr6:29585121:> Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr6:29,552,898-29,558,277 |
| hg38 | chr6:29,585,121-29,590,500 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
[No Data.]
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 | hyperinsulinism | NA | BeFree | Detail | |
| 0.003 | Lupus Erythematosus, Systemic | NA | BeFree,GAD | Detail | |
| 0.002 | multiple sclerosis | NA | GAD | Detail | |
| 0.003 | Lupus Erythematosus, Systemic | Sequential removal of SLE-associated DRB1 haplotypes revealed independent effect... | BeFree | 19851445 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| Sequential removal of SLE-associated DRB1 haplotypes revealed independent effects due to variation w... | DisGeNET | Detail |
Overlapped Transcript Coordinates
| Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
|---|
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs10947345 dbSNP
- Genome
- hg38
- Position
- chr6:29,585,121-29,590,500
- Variant Type
- snv
Genome browser