SERPINB5, serpin family B member 5, 5268

N. diseases: 87; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6567365
rs6567365
Entrez Id: 5268;100505704
Gene Symbol: SERPINB5;ATP5MC1P6
SERPINB5;ATP5MC1P6
CUI: C0027404
Disease:
Narcolepsy 		0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009
dbSNP: rs17071138
rs17071138
Entrez Id: 5268
Gene Symbol: SERPINB5
SERPINB5
CUI: C0153381
Disease:
Malignant neoplasm of mouth 		0.010 GeneticVariation BEFREE Heterozygous TC of the SERPINB5 rs17071138 polymorphism may be a factor that increases susceptibility to oral cancer. 28339463 2017
dbSNP: rs17071138
rs17071138
Entrez Id: 5268
Gene Symbol: SERPINB5
SERPINB5
CUI: C0220641
Disease:
Lip and Oral Cavity Carcinoma 		0.010 GeneticVariation BEFREE Heterozygous TC of the SERPINB5 rs17071138 polymorphism may be a factor that increases susceptibility to oral cancer. 28339463 2017
dbSNP: rs8089104
rs8089104
Entrez Id: 5268
Gene Symbol: SERPINB5
SERPINB5
CUI: C0153381
Disease:
Malignant neoplasm of mouth 		0.010 GeneticVariation BEFREE We found that individuals carrying the polymorphic rs17071138 and rs8089104 are more susceptible to oral cancer (OR, 1.57; 95% CI, 1.07~2.31 and OR, 1.58; 95% CI, 1.04~2.39, respectively). 28339463 2017
dbSNP: rs8089104
rs8089104
Entrez Id: 5268
Gene Symbol: SERPINB5
SERPINB5
CUI: C0220641
Disease:
Lip and Oral Cavity Carcinoma 		0.010 GeneticVariation BEFREE We found that individuals carrying the polymorphic rs17071138 and rs8089104 are more susceptible to oral cancer (OR, 1.57; 95% CI, 1.07~2.31 and OR, 1.58; 95% CI, 1.04~2.39, respectively). 28339463 2017
dbSNP: rs2289520
rs2289520
Entrez Id: 5268
Gene Symbol: SERPINB5
SERPINB5
CUI: C0220641
Disease:
Lip and Oral Cavity Carcinoma 		0.010 GeneticVariation BEFREE G allele of Maspin rs2289520 polymorphism may be a factor that increases the susceptibility to oral cancer. 27525723 2016
dbSNP: rs2289520
rs2289520
Entrez Id: 5268
Gene Symbol: SERPINB5
SERPINB5
CUI: C0153381
Disease:
Malignant neoplasm of mouth 		0.010 GeneticVariation BEFREE G allele of Maspin rs2289520 polymorphism may be a factor that increases the susceptibility to oral cancer. 27525723 2016
dbSNP: rs2289519
rs2289519
Entrez Id: 5268
Gene Symbol: SERPINB5
SERPINB5
CUI: C0279626
Disease:
Squamous cell carcinoma of esophagus 		0.010 GeneticVariation BEFREE Haplotype analysis showed that the T-G haplotype (corresponding to rs2289519-rs2289520) increased the risk of ESCC, while the C-C haplotype decreased the risk. 25775950 2015
dbSNP: rs2289520
rs2289520
Entrez Id: 5268
Gene Symbol: SERPINB5
SERPINB5
CUI: C0279626
Disease:
Squamous cell carcinoma of esophagus 		0.010 GeneticVariation BEFREE Haplotype analysis showed that the T-G haplotype (corresponding to rs2289519-rs2289520) increased the risk of ESCC, while the C-C haplotype decreased the risk. 25775950 2015