chr22:25588025:C>T Detail (hg38) (GRK3)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr22:25,983,992-25,983,992 View the variant detail on this assembly version. |
hg38 | chr22:25,588,025-25,588,025 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_005160.3:c.114-16352C>T | |
Ensemble | ENST00000324198.11:c.114-16352C>T |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.008 | Malignant neoplasm of urinary bladder | In the meta-analysis, the reported risk allele for four SNPs were significantly ... | BeFree | 22711262 | Detail |
0.004 | Carcinoma of bladder | In the meta-analysis, the reported risk allele for four SNPs were significantly ... | BeFree | 22711262 | Detail |
0.129 | Malignant neoplasm of urinary bladder | In the meta-analysis, the reported risk allele for four SNPs were significantly ... | BeFree | 22711262 | Detail |
0.007 | Carcinoma of bladder | In the meta-analysis, the reported risk allele for four SNPs were significantly ... | BeFree | 22711262 | Detail |
0.012 | Malignant neoplasm of urinary bladder | In the meta-analysis, the reported risk allele for four SNPs were significantly ... | BeFree | 22711262 | Detail |
0.123 | Malignant neoplasm of urinary bladder | In the meta-analysis, the reported risk allele for four SNPs were significantly ... | BeFree | 22711262 | Detail |
<0.001 | Carcinoma of bladder | In the meta-analysis, the reported risk allele for four SNPs were significantly ... | BeFree | 22711262 | Detail |
0.003 | Carcinoma of bladder | In the meta-analysis, the reported risk allele for four SNPs were significantly ... | BeFree | 22711262 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
In the meta-analysis, the reported risk allele for four SNPs were significantly associated with incr... | DisGeNET | Detail |
In the meta-analysis, the reported risk allele for four SNPs were significantly associated with incr... | DisGeNET | Detail |
In the meta-analysis, the reported risk allele for four SNPs were significantly associated with incr... | DisGeNET | Detail |
In the meta-analysis, the reported risk allele for four SNPs were significantly associated with incr... | DisGeNET | Detail |
In the meta-analysis, the reported risk allele for four SNPs were significantly associated with incr... | DisGeNET | Detail |
In the meta-analysis, the reported risk allele for four SNPs were significantly associated with incr... | DisGeNET | Detail |
In the meta-analysis, the reported risk allele for four SNPs were significantly associated with incr... | DisGeNET | Detail |
In the meta-analysis, the reported risk allele for four SNPs were significantly associated with incr... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs9624880 dbSNP
- Genome
- hg38
- Position
- chr22:25,588,025-25,588,025
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
Genome browser