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.

    Edit (Admin) | Delete