rs1800392

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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