chr5:26880706:> Detail (hg19)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr5:26,880,706-27,038,693 |
| hg38 | chr5:26,880,597-27,038,586 |
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 |
|---|---|---|---|---|---|
| <0.001 | obsessive-compulsive disorder | NA | BeFree | Detail | |
| <0.001 | osteochondritis dissecans | NA | BeFree | Detail | |
| <0.001 | renal fibrosis | NA | BeFree | Detail | |
| <0.001 | anorexia nervosa | Five SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empiri... | BeFree | 23337130 | Detail |
| <0.001 | obsessive-compulsive disorder | Five SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empiri... | BeFree | 23337130 | Detail |
| <0.001 | osteochondritis dissecans | Five SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empiri... | BeFree | 23337130 | Detail |
| 0.002 | Creatinine finding | NA | GAD | Detail | |
| 0.002 | Glomerular filtration rate finding | NA | GAD | Detail | |
| <0.001 | anorexia nervosa | NA | BeFree | Detail | |
| 0.122 | autistic disorder | NA | CTD_human,GAD | Detail | |
| <0.001 | renal cell carcinoma | NA | BeFree | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| Five SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-va... | DisGeNET | Detail |
| Five SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-va... | DisGeNET | Detail |
| Five SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-va... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | 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
- rs1074815 dbSNP
- Genome
- hg19
- Position
- chr5:26,880,706-27,038,693
- Variant Type
- snv
Genome browser