chr15:78856266:C>T Detail (hg19)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr15:78,856,266-78,856,266 |
| hg38 | chr15:78,563,924-78,563,924 View the variant detail on this assembly version. |
HGVS
[No Data.]
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:[No Data.] |
| ToMMo:0.091 | |
| 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 |
|---|---|---|---|---|---|
| 0.327 | Lung Neoplasms | We found that four of the variants (rs3829787, rs3841324, rs588765 and rs3743073... | BeFree | 23011884 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| We found that four of the variants (rs3829787, rs3841324, rs588765 and rs3743073) were associated wi... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs3829787 dbSNP
- Genome
- hg19
- Position
- chr15:78,856,266-78,856,266
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
- 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))
- rs3829787
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.0915
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 1534
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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