Polymorphism: rs1346044
rs1346044
(
SNPedia |
23andMe
)
Alias: Cys1367Arg
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:
Initial study (Finish cohort): 175 vs 178. Other cohorts: Mexican newborns 169, USA adults (48) 23, Japanese adults (53) 198.
Trivial name is Cys1367Arg.
Ethnicity:
Finn
Age of cases: 100.8
Finding: Negative
Statistics
- Number of cases/controls: 175 vs 178 (initial)
- Significant: Yes
Study Design
- Study type: Candidate Region/Gene
- Technology: Multilocus PCR
Reference:
10069711: Polymorphisms at the Werner locus: I. Newly identified polymorphisms, ethnic variability of 1367Cys/Arg, and its stability in a population of Finnish centenarians.
Choice: Clean
Created: June 30, 2013, midnight
Updated: Aug. 8, 2014, 1:05 p.m.
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