chr12:48417317:> Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr12:48,811,100-48,811,100 |
| hg38 | chr12:48,417,317-48,417,317 |
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
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| A genome-wide search for loci interacting with known prostate cancer risk-associated genetic variant... | GWAS Catalog | 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
- rs4489787 dbSNP
- Genome
- hg38
- Position
- chr12:48,417,317-48,417,317
- Variant Type
- snv
Genome browser