chr7:22765456:G>T Detail (hg19)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr7:22,765,456-22,765,456 |
| hg38 | chr7:22,725,837-22,725,837 View the variant detail on this assembly version. |
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 | systemic scleroderma | In the IL6 allelic combination analyses, the GGC allelic combination rs2069827-r... | BeFree | 23027890 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| In the IL6 allelic combination analyses, the GGC allelic combination rs2069827-rs1800795-rs2069840 s... | 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
- rs2069827 dbSNP
- Genome
- hg19
- Position
- chr7:22,765,456-22,765,456
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- T
Genome browser