chr12:53500681:G>A Detail (hg38)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr12:53,894,465-53,894,465 View the variant detail on this assembly version. |
hg38 | chr12:53,500,681-53,500,681 |
HGVS
[No Data.]
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | 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 | chronic lymphocytic leukemia | We found nine statistically significant associations with CLL risk after FDR cor... | BeFree | 25793711 | Detail |
<0.001 | chronic lymphocytic leukemia | We found nine statistically significant associations with CLL risk after FDR cor... | BeFree | 25793711 | Detail |
<0.001 | chronic lymphocytic leukemia | We found nine statistically significant associations with CLL risk after FDR cor... | BeFree | 25793711 | Detail |
<0.001 | chronic lymphocytic leukemia | We found nine statistically significant associations with CLL risk after FDR cor... | BeFree | 25793711 | Detail |
<0.001 | chronic lymphocytic leukemia | We found nine statistically significant associations with CLL risk after FDR cor... | BeFree | 25793711 | Detail |
<0.001 | chronic lymphocytic leukemia | We found nine statistically significant associations with CLL risk after FDR cor... | BeFree | 25793711 | Detail |
<0.001 | chronic lymphocytic leukemia | We found nine statistically significant associations with CLL risk after FDR cor... | BeFree | 25793711 | Detail |
<0.001 | chronic lymphocytic leukemia | We found nine statistically significant associations with CLL risk after FDR cor... | BeFree | 25793711 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
We found nine statistically significant associations with CLL risk after FDR correction, seven in mi... | DisGeNET | Detail |
We found nine statistically significant associations with CLL risk after FDR correction, seven in mi... | DisGeNET | Detail |
We found nine statistically significant associations with CLL risk after FDR correction, seven in mi... | DisGeNET | Detail |
We found nine statistically significant associations with CLL risk after FDR correction, seven in mi... | DisGeNET | Detail |
We found nine statistically significant associations with CLL risk after FDR correction, seven in mi... | DisGeNET | Detail |
We found nine statistically significant associations with CLL risk after FDR correction, seven in mi... | DisGeNET | Detail |
We found nine statistically significant associations with CLL risk after FDR correction, seven in mi... | DisGeNET | Detail |
We found nine statistically significant associations with CLL risk after FDR correction, seven in mi... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs784567 dbSNP
- Genome
- hg38
- Position
- chr12:53,500,681-53,500,681
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- A
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