chr11:102715949:>C Detail (hg19)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr11:102,715,949-102,715,949 |
hg38 | chr11:102,845,218-102,845,218 |
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 |
---|---|---|---|---|---|
0.009 | Malignant neoplasm of lung | We investigated the associations between polymorphisms of MMP-1 (-1607 1G/2G, rs... | BeFree | 16311244 | Detail |
0.002 | Carcinoma of lung | We investigated the associations between polymorphisms of MMP-1 (-1607 1G/2G, rs... | BeFree | 16311244 | Detail |
0.001 | Carcinoma of lung | We investigated the associations between polymorphisms of MMP-1 (-1607 1G/2G, rs... | BeFree | 16311244 | Detail |
0.016 | Malignant neoplasm of lung | We investigated the associations between polymorphisms of MMP-1 (-1607 1G/2G, rs... | BeFree | 16311244 | Detail |
0.004 | aortic aneurysm | For SNPs that had previously been associated with AAA presence, meta-analysis of... | BeFree | 24613192 | Detail |
0.002 | aortic aneurysm | For SNPs that had previously been associated with AAA presence, meta-analysis of... | BeFree | 24613192 | Detail |
0.003 | Aneurysm | Analysis of the five MMP genes identified modest trends in allele and genotype f... | BeFree | 20827277 | Detail |
0.004 | Aneurysm | Analysis of the five MMP genes identified modest trends in allele and genotype f... | BeFree | 20827277 | Detail |
0.046 | myocardial infarction | We conducted a haplotype analysis to examine the role of common variation of MMP... | BeFree | 19762026 | Detail |
0.003 | Moyamoya disease | MDR analysis failed to detect any significant interaction among these five loci ... | BeFree | 23769926 | Detail |
<0.001 | Moyamoya disease 1 | MDR analysis failed to detect any significant interaction among these five loci ... | BeFree | 23769926 | Detail |
<0.001 | Moyamoya disease 1 | MDR analysis failed to detect any significant interaction among these five loci ... | BeFree | 23769926 | Detail |
<0.001 | Moyamoya disease | MDR analysis failed to detect any significant interaction among these five loci ... | BeFree | 23769926 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
We investigated the associations between polymorphisms of MMP-1 (-1607 1G/2G, rs1799750), MMP-3 (-11... | DisGeNET | Detail |
We investigated the associations between polymorphisms of MMP-1 (-1607 1G/2G, rs1799750), MMP-3 (-11... | DisGeNET | Detail |
We investigated the associations between polymorphisms of MMP-1 (-1607 1G/2G, rs1799750), MMP-3 (-11... | DisGeNET | Detail |
We investigated the associations between polymorphisms of MMP-1 (-1607 1G/2G, rs1799750), MMP-3 (-11... | DisGeNET | Detail |
For SNPs that had previously been associated with AAA presence, meta-analysis of currently available... | DisGeNET | Detail |
For SNPs that had previously been associated with AAA presence, meta-analysis of currently available... | DisGeNET | Detail |
Analysis of the five MMP genes identified modest trends in allele and genotype frequencies for MMP-3... | DisGeNET | Detail |
Analysis of the five MMP genes identified modest trends in allele and genotype frequencies for MMP-3... | DisGeNET | Detail |
We conducted a haplotype analysis to examine the role of common variation of MMP3 in myocardial infa... | DisGeNET | Detail |
MDR analysis failed to detect any significant interaction among these five loci in the occurrence of... | DisGeNET | Detail |
MDR analysis failed to detect any significant interaction among these five loci in the occurrence of... | DisGeNET | Detail |
MDR analysis failed to detect any significant interaction among these five loci in the occurrence of... | DisGeNET | Detail |
MDR analysis failed to detect any significant interaction among these five loci in the occurrence of... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs3025058 dbSNP
- Genome
- hg19
- Position
- chr11:102,715,949-102,715,949
- Variant Type
- snv
- Reference Allele
- -
- Alternative Allele
- C
Genome browser