TREH, trehalase, 11181

N. diseases: 42; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17748
rs17748
Entrez Id: 11181;23187
Gene Symbol: TREH;PHLDB1
TREH;PHLDB1
CUI: C0017638
Disease:
Glioma
0.710 GeneticVariation BEFREE Overall, we found three protective alleles for glioma in patients: the allele "G" of rs1801275 in the IL4R gene by allele model (odds ratio [OR], 0.71; 95% confidence interval [CI], 0.50-0.99; P=0.04) and dominant model (OR, 0.67; 95% CI, 0.46-0.99; P=0.04) analysis respectively, the allele "T" of rs17748 in the TREH gene by recessive model (OR, 0.48; 95% CI, 0.23-1.01; P=0.05) analysis, and the allele "G" of rs6470745 in CCDC26 gene by recessive model (OR, 0.48; 95% CI, 0.26-0.89; P=0.02) analysis. 22369735 2012
dbSNP: rs17748
rs17748
Entrez Id: 11181;23187
Gene Symbol: TREH;PHLDB1
TREH;PHLDB1
CUI: C0017638
Disease:
Glioma
0.710 GeneticVariation GWASDB Chromosome 7p11.2 (EGFR) variation influences glioma risk. 21531791 2011
dbSNP: rs17748
rs17748
Entrez Id: 11181;23187
Gene Symbol: TREH;PHLDB1
TREH;PHLDB1
CUI: C0017638
Disease:
Glioma
0.710 GeneticVariation GWASDB Genome-wide association study identifies five susceptibility loci for glioma. 19578367 2009
dbSNP: rs506234
rs506234
Entrez Id: 11181
Gene Symbol: TREH
TREH
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement
C 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs507080
rs507080
Entrez Id: 11181
Gene Symbol: TREH
TREH
CUI: C0523465
Disease:
Serum albumin measurement
A 0.700 GeneticVariation GWASDB Genetic determinants influencing human serum metabolome among African Americans. 24625756 2014
dbSNP: rs527655595
rs527655595
Entrez Id: 11181
Gene Symbol: TREH
TREH
CUI: C0268187
Disease:
alpha, alpha-Trehalase deficiency
C 0.700 CausalMutation CLINVAR
dbSNP: rs17748
rs17748
Entrez Id: 11181;23187
Gene Symbol: TREH;PHLDB1
TREH;PHLDB1
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE Our results suggested that rs1059122 (FAM13A), rs17748 (PHLDB1), and rs4809957 (CYP24A1) might contribute to breast cancer susceptibility in the Chinese Han population. 31215377 2019
dbSNP: rs17748
rs17748
Entrez Id: 11181;23187
Gene Symbol: TREH;PHLDB1
TREH;PHLDB1
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE Our results suggested that rs1059122 (FAM13A), rs17748 (PHLDB1), and rs4809957 (CYP24A1) might contribute to breast cancer susceptibility in the Chinese Han population. 31215377 2019
dbSNP: rs7389
rs7389
Entrez Id: 11181;23187
Gene Symbol: TREH;PHLDB1
TREH;PHLDB1
CUI: C0017661
Disease:
IGA Glomerulonephritis
0.010 GeneticVariation BEFREE As a result, NTN4 rs1362970 A/A and GNG2 rs3204008 G/G genotypes were associated with enhanced IgAN risk in males (p = 0.006, p = 0.023, respectively), and the association between the PHLDB1 rs7389 G/T genotype and higher IgAN risk was found in females (p = 0.008). 30928649 2019
dbSNP: rs17748
rs17748
Entrez Id: 11181;23187
Gene Symbol: TREH;PHLDB1
TREH;PHLDB1
CUI: C0017636
Disease:
Glioblastoma
0.010 GeneticVariation BEFREE The variant TT genotype of TREH rs17748 and the variant TT genotype of PHLDB1 rs498872 decreased GBM risk in the recessive model. 26156397 2015
dbSNP: rs17748
rs17748
Entrez Id: 11181;23187
Gene Symbol: TREH;PHLDB1
TREH;PHLDB1
CUI: C1621958
Disease:
Glioblastoma Multiforme
0.010 GeneticVariation BEFREE The variant TT genotype of TREH rs17748 and the variant TT genotype of PHLDB1 rs498872 decreased GBM risk in the recessive model. 26156397 2015