chr2:47703500:T>G Detail (hg19) (MSH2)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr2:47,703,500-47,703,500 |
| hg38 | chr2:47,476,361-47,476,361 |
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 |
|---|---|---|
| The genetic variant rs2303428 (MSH2) might serve as a predictive marker for chemotherapy response (t... | MMMP | Detail |
| The genetic variant rs2303428 (MSH2) might serve as a predictive marker for chemotherapy response (t... | MMMP | Detail |
| The genetic variant rs2303428 (MSH2) might serve as a predictive marker for hematologic side effects | MMMP | Detail |
| The genetic variant rs2303428 (MSH2) might serve as a predictive marker for hematologic side effects | MMMP | Detail |
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- Genome
- hg19
- Position
- chr2:47,703,500-47,703,500
- Variant Type
- snv
- Reference Allele
- T
- Alternative Allele
- G
- MMMP State (molecule) (MMMP)
- polymorphism rs2303428
Genome browser