|
rs4968451
|
|
Adult Meningioma
|
|
0.020 |
GeneticVariation
|
BEFREE |
The polymorphisms rs4968451T>G in BRIP1 were significantly associated with the risk of meningioma (TT vs. TG vs. GG additive, P = 0.005; TT+TG vs. GG dominant, P = 0.015; TT/GT+GG recessive, P = 0.034).
|
29581016 |
2018 |
|
rs4968451
|
|
Meningioma
|
|
0.020 |
GeneticVariation
|
BEFREE |
The polymorphisms rs4968451T>G in BRIP1 were significantly associated with the risk of meningioma (TT vs. TG vs. GG additive, P = 0.005; TT+TG vs. GG dominant, P = 0.015; TT/GT+GG recessive, P = 0.034).
|
29581016 |
2018 |
|
rs4968451
|
|
Meningioma, benign, no ICD-O subtype
|
|
0.020 |
GeneticVariation
|
BEFREE |
The polymorphisms rs4968451T>G in BRIP1 were significantly associated with the risk of meningioma (TT vs. TG vs. GG additive, P = 0.005; TT+TG vs. GG dominant, P = 0.015; TT/GT+GG recessive, P = 0.034).
|
29581016 |
2018 |
|
rs4968451
|
|
Meningioma, benign, no ICD-O subtype
|
|
0.020 |
GeneticVariation
|
BEFREE |
We have identified a novel association between rs4968451 and meningioma risk.
|
18270339 |
2008 |
|
rs4968451
|
|
Adult Meningioma
|
|
0.020 |
GeneticVariation
|
BEFREE |
We have identified a novel association between rs4968451 and meningioma risk.
|
18270339 |
2008 |
|
rs4968451
|
|
Meningioma
|
|
0.020 |
GeneticVariation
|
BEFREE |
We have identified a novel association between rs4968451 and meningioma risk.
|
18270339 |
2008 |
|
rs4968451
|
|
Grade I Meningioma
|
|
0.010 |
GeneticVariation
|
BEFREE |
BRIP1 rs4968451T>G was associated with markedly grade I meningioma risk (TT+TG vs. GG dominant, P = 0.008; TT/GT+GG recessive, P = 0.020).
|
29581016 |
2018 |
|
rs4968451
|
|
Adult Grade I Meningioma
|
|
0.010 |
GeneticVariation
|
BEFREE |
BRIP1 rs4968451T>G was associated with markedly grade I meningioma risk (TT+TG vs. GG dominant, P = 0.008; TT/GT+GG recessive, P = 0.020).
|
29581016 |
2018 |
|
rs4968451
|
|
Childhood Grade I Meningioma
|
|
0.010 |
GeneticVariation
|
BEFREE |
BRIP1 rs4968451T>G was associated with markedly grade I meningioma risk (TT+TG vs. GG dominant, P = 0.008; TT/GT+GG recessive, P = 0.020).
|
29581016 |
2018 |
|
rs4968451
|
|
Neoplasms
|
|
0.010 |
GeneticVariation
|
BEFREE |
Through genotype-phenotype analysis, the genotype of BRIP1 rs4968451T>G was also strongly associated with tumor-related phenotypes, including the tumor grade and tumor subtypes.
|
29581016 |
2018 |
|
rs4968451
|
|
Transitional Meningioma
|
|
0.010 |
GeneticVariation
|
BEFREE |
In addition, BRIP1 rs4968451T>G was associated with markedly meningothelial and transitional meningioma risk.
|
29581016 |
2018 |
|
rs4968451
|
|
Cervix carcinoma
|
|
0.010 |
GeneticVariation
|
BEFREE |
The results showed that rs16945692 (intron 1), rs4968451 (intron 4), rs4986764 (exon 18) and rs7213430 (3'UTR) were significantly associated with cervical cancer (P<0.05).
|
23644138 |
2013 |
|
rs4968451
|
|
Malignant tumor of cervix
|
|
0.010 |
GeneticVariation
|
BEFREE |
The results showed that rs16945692 (intron 1), rs4968451 (intron 4), rs4986764 (exon 18) and rs7213430 (3'UTR) were significantly associated with cervical cancer (P<0.05).
|
23644138 |
2013 |
|
rs4968451
|
|
cervical cancer
|
|
0.010 |
GeneticVariation
|
BEFREE |
The results showed that rs16945692 (intron 1), rs4968451 (intron 4), rs4986764 (exon 18) and rs7213430 (3'UTR) were significantly associated with cervical cancer (P<0.05).
|
23644138 |
2013 |
|
rs4968451
|
|
Breast Carcinoma
|
|
0.010 |
GeneticVariation
|
BEFREE |
The SNP rs4968451, which maps to intron 4 of the gene that encodes breast cancer susceptibility gene 1-interacting protein 1, was consistently associated with an increased risk of developing meningioma.
|
18270339 |
2008 |
|
rs4968451
|
|
Malignant neoplasm of breast
|
|
0.010 |
GeneticVariation
|
BEFREE |
The SNP rs4968451, which maps to intron 4 of the gene that encodes breast cancer susceptibility gene 1-interacting protein 1, was consistently associated with an increased risk of developing meningioma.
|
18270339 |
2008 |