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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