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Longevity DB
Genetic variants implicated in human longevity.
Polymorphism:
rs3212948
rs3212948
(
SNPedia
|
23andMe
)
Location:
19q13.32
Factor:
- Symbol:
ERCC1
- Name:
excision repair cross-complementing rodent repair deficiency, complementation group 1 (includes overlapping antisense sequence)
- Entrez ID:
2067
- Ensembl ID:
ENSG00000012061
Factors:
ERCC1
excision repair cross-complementing rodent repair deficiency, complementation group 1 (includes overlapping antisense sequence)
(
2067
/
ENSG00000012061
)
Ethnicity:
Calabrian
Age of cases:
90+, median 92
Statistics
- Number of cases/controls:
288 vs 554 (initial)
- p-value:
0.1062 [0.1062]
- Significant:
No
Study Design
- Classifications:
No Age Effect
- Study type:
Candidate Region/Gene
- Technology:
allele-specific PCR-based KASPar SNP genotyping system (KBiosciences, Hoddesdon, UK) (Cuppen
Reference:
22576335: MAP3K7 and GSTZ1 are associated with human longevity: a two-stage case-control study using a multilocus genotyping.
Choice:
Curate
Created:
July 2, 2013, 2:48 a.m.
Updated:
Aug. 8, 2014, 1:06 p.m.
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