chr2:204738919:G>T Detail (hg19) (CTLA4)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr2:204,738,919-204,738,919 |
| hg38 | chr2:203,874,196-203,874,196 |
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
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| Influence of cytotoxic T lymphocyte-associated antigen 4 (CTLA4) common polymorphisms on outcome in ... | MMMP | Detail |
- Gene
- -
- Genome
- hg19
- Position
- chr2:204,738,919-204,738,919
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- T
- MMMP State (molecule) (MMMP)
- polymorphism rs3087243
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