chr12:13981909:C>A Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr12:14,134,843-14,134,843 View the variant detail on this assembly version. |
| hg38 | chr12:13,981,909-13,981,909 |
HGVS
[No Data.]
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:[No Data.] |
| ToMMo:0.534 | |
| NCBN:[No Data.] | |
| NCBN(Hondo):[No Data.] | |
| NCBN(Ryukyu):[No Data.] | |
| East asia | ExAC:[No Data.] |
Prediction
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 | Drug habituation | According to this practical and scientific demand, we aimed to investigate the r... | BeFree | 20421849 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| According to this practical and scientific demand, we aimed to investigate the relationship between ... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs1019385 dbSNP
- Genome
- hg38
- Position
- chr12:13,981,909-13,981,909
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- A
- ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- PASS
- Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- rs1019385
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.5339
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 8946
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16756
Genome browser