chr8:143751864:G>A Detail (hg19)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr8:143,751,864-143,751,864 |
| hg38 | chr8:142,670,446-142,670,446 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:0.243 | |
| 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 | gallbladder carcinoma | PSCA gene variants (rs2294008 and rs2978974) confer increased susceptibility of ... | BeFree | 23988503 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| PSCA gene variants (rs2294008 and rs2978974) confer increased susceptibility of gallbladder carcinom... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs2978974 dbSNP
- Genome
- hg19
- Position
- chr8:143,751,864-143,751,864
- Variant Type
- snv
- Reference Allele
- G
- 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))
- rs2978974
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.2433
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 4077
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
Genome browser