chr7:100769706:>G Detail (hg19)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr7:100,769,706-100,769,706 |
hg38 | chr7:101,126,425-101,126,425 |
HGVS
Type | Transcript | Protein |
---|---|---|
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
[No Data.]
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 | Metabolic syndrome X | In a marker-by-marker analysis, the ADRB2 rs180088 (OR 1.22, 95% CI 1.01-1.48) a... | BeFree | 19619703 | Detail |
0.016 | Metabolic syndrome X | In postmenopausal women, an increased MetS risk was found for the ADRB2 rs180088... | BeFree | 19619703 | Detail |
0.015 | Metabolic syndrome X | In postmenopausal women, an increased MetS risk was found for the ADRB2 rs180088... | BeFree | 19619703 | Detail |
0.013 | Metabolic syndrome X | In postmenopausal women, an increased MetS risk was found for the ADRB2 rs180088... | BeFree | 19619703 | Detail |
0.003 | Metabolic syndrome X | In postmenopausal women, an increased MetS risk was found for the ADRB2 rs180088... | BeFree | 19619703 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
In a marker-by-marker analysis, the ADRB2 rs180088 (OR 1.22, 95% CI 1.01-1.48) and PAI1 rs1799768 (O... | DisGeNET | Detail |
In postmenopausal women, an increased MetS risk was found for the ADRB2 rs180088 (OR 1.28, 95% CI 0.... | DisGeNET | Detail |
In postmenopausal women, an increased MetS risk was found for the ADRB2 rs180088 (OR 1.28, 95% CI 0.... | DisGeNET | Detail |
In postmenopausal women, an increased MetS risk was found for the ADRB2 rs180088 (OR 1.28, 95% CI 0.... | DisGeNET | Detail |
In postmenopausal women, an increased MetS risk was found for the ADRB2 rs180088 (OR 1.28, 95% CI 0.... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs1799768 dbSNP
- Genome
- hg19
- Position
- chr7:100,769,706-100,769,706
- Variant Type
- snv
- Reference Allele
- -
- Alternative Allele
- G
Genome browser