chr19:10289434:G>C Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr19:10,400,110-10,400,110 View the variant detail on this assembly version. |
| hg38 | chr19:10,289,434-10,289,434 |
HGVS
[No Data.]
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:[No Data.] |
| ToMMo:0.465 | |
| 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 | Malignant neoplasm of breast | Our meta-analysis suggests that the ICAM5 V301I and rs281439 variants but not IC... | BeFree | 23079714 | Detail |
| 0.006 | Malignant neoplasm of breast | Our meta-analysis suggests that the ICAM5 V301I and rs281439 variants but not IC... | BeFree | 23079714 | Detail |
| <0.001 | breast carcinoma | Our meta-analysis suggests that the ICAM5 V301I and rs281439 variants but not IC... | BeFree | 23079714 | Detail |
| 0.004 | breast carcinoma | Our meta-analysis suggests that the ICAM5 V301I and rs281439 variants but not IC... | BeFree | 23079714 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| Our meta-analysis suggests that the ICAM5 V301I and rs281439 variants but not ICAM1 K469E polymorphi... | DisGeNET | Detail |
| Our meta-analysis suggests that the ICAM5 V301I and rs281439 variants but not ICAM1 K469E polymorphi... | DisGeNET | Detail |
| Our meta-analysis suggests that the ICAM5 V301I and rs281439 variants but not ICAM1 K469E polymorphi... | DisGeNET | Detail |
| Our meta-analysis suggests that the ICAM5 V301I and rs281439 variants but not ICAM1 K469E polymorphi... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs281439 dbSNP
- Genome
- hg38
- Position
- chr19:10,289,434-10,289,434
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- C
- 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))
- rs281439
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.4653
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 7799
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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