chr22:37256846:G>T Detail (hg19) (NCF4)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr22:37,256,846-37,256,846 |
| hg38 | chr22:36,860,804-36,860,804 |
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 |
|---|---|---|
| Non melanoma specific model (lymphoma). Increased cardiotoxicity. Phase III RCT comparing variants o... | MMMP | Detail |
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- Genome
- hg19
- Position
- chr22:37,256,846-37,256,846
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- T
- MMMP State (molecule) (MMMP)
- genotype A/A of polymorphism rs1883112
Genome browser