rs1061170

Polymorphism: rs1061170
rs1061170 ( SNPedia | 23andMe )

Variant Type: SNP
Location: 1q32

Factor:
- Symbol: CFH
- Name: complement factor H
- Entrez ID: 3075
- Ensembl ID: ENSG00000000971

Factors:
  • CFH complement factor H ( 3075 / ENSG00000000971 )

  • Ethnicity: Finn
    Shorter lived allele: His
    Finding: Positive

    Statistics
    - Number of cases/controls: 491 vs 0 (initial)
    - Odds ratio: 1.78
    - p-value: 0.005 [0.005]
    - Significant: yes

    Study Design
    - Classifications: Longevity-Associated
    - Technology: N/A

    Reference:
    19000922: Complement factor H 402His variant confers an increased mortality risk in Finnish nonagenarians: the Vitality 90+ study.

    Choice: Curate
    Created: July 2, 2013, 2:47 a.m.
    Updated: Aug. 10, 2014, 12:01 a.m.

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