Polymorphism: rs1800392
rs1800392
(
SNPedia |
23andMe
)
Variant Type: SNP
Factor:
- Symbol: WRN
- Name: Werner syndrome, RecQ helicase-like
- Entrez ID: 7486
- Ensembl ID: ENSG00000165392
Factors:
WRN
Werner syndrome, RecQ helicase-like
(
7486
/
ENSG00000165392
)
Ethnicity:
Multiethnic
Age of cases: 100
Finding: Positive
Statistics
- Number of cases/controls: 2715 vs 2725 (initial)
- Odds ratio: 0.787
- Odds ratio type:
- p-value:
0.000708
[0.000708]
- Significant: Yes
Study Design
- Classifications:
Longevity-Associated
- Study type: Meta-Analysis
- Technology:
Reference:
24244950: Meta‐analysis of genetic variants associated with human exceptional longevity.
Choice: Curate
Created: Aug. 31, 2014, 9:35 p.m.
Updated: Aug. 31, 2014, 9:35 p.m.
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