Polymorphism: rs3087425
rs3087425
(
SNPedia |
23andMe
)
Variant Type: SNP
Location: 8p12
Factor:
- Symbol: WRN
- Name: Werner syndrome, RecQ helicase-like
- Entrez ID: 7486
- Ensembl ID: ENSG00000165392
Factors:
WRN
Werner syndrome, RecQ helicase-like
(
7486
/
ENSG00000165392
)
Description:
Therefore, we suggest that the analyzed polymorphic variants of the WRN influence neither the rate of aging nor the longevity.
Trivial name is R834C.
Ethnicity:
Polish
Age of cases: Mean age 101.1
Finding: Negative
Statistics
- Number of cases/controls: 149 vs 414 (initial)
- Significant: No
Study Design
- Classifications:
No Age Effect
- Study type: Candidate Region/Gene
- Technology: PCR
Reference:
20855428: Aging is accompanied by a progressive decrease of expression of the WRN gene in human blood mononuclear cells.
Choice: Clean
Created: July 1, 2013, 1:04 p.m.
Updated: Aug. 8, 2014, 1:05 p.m.
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