chr15:69726651:A>G Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr15:70,018,990-70,018,990 View the variant detail on this assembly version. |
| hg38 | chr15:69,726,651-69,726,651 |
HGVS
[No Data.]
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:[No Data.] |
| ToMMo:0.716 | |
| 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 |
|---|---|---|---|---|---|
| 0.002 | chronic lymphocytic leukemia | [A genome-wide association study identifies six susceptibility loci for chronic ... | GAD | 18758461 | Detail |
| 0.250 | chronic lymphocytic leukemia | We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2... | GWASCAT | 18758461 | Detail |
| 0.248 | chronic lymphocytic leukemia | We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2... | BeFree | 18758461 | Detail |
| 0.254 | chronic lymphocytic leukemia | We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2... | BeFree | 18758461 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| [A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia... | DisGeNET | Detail |
| We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37... | DisGeNET | Detail |
| We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37... | DisGeNET | Detail |
| We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37... | DisGeNET | Detail |
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs7176508 dbSNP
- Genome
- hg38
- Position
- chr15:69,726,651-69,726,651
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- G
- 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))
- rs7176508
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.7165
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 12009
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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