chr3:191728221:>TA Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr3:191,446,010-191,446,010 |
| hg38 | chr3:191,728,221-191,728,221 |
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 |
|---|---|---|---|---|---|
| 0.033 | colorectal cancer | Of note, the MGMT Lys(178)Arg (rs2308237) SNP, in linkage disequilibrium with th... | BeFree | 18268114 | Detail |
| 0.014 | colorectal carcinoma | Of note, the MGMT Lys(178)Arg (rs2308237) SNP, in linkage disequilibrium with th... | BeFree | 18268114 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| Of note, the MGMT Lys(178)Arg (rs2308237) SNP, in linkage disequilibrium with the previously reporte... | DisGeNET | Detail |
| Of note, the MGMT Lys(178)Arg (rs2308237) SNP, in linkage disequilibrium with the previously reporte... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs2308237 dbSNP
- Genome
- hg38
- Position
- chr3:191,728,221-191,728,221
- Variant Type
- snv
- Reference Allele
- -
- Alternative Allele
- TA
Genome browser