CTSB, cathepsin B, 1508

N. diseases: 304; N. variants: 17
Disease: Diabetes ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs747940576
rs747940576
Entrez Id: 1508
Gene Symbol: CTSB
CTSB
CUI: C0011847
Disease:
Diabetes 		0.010 GeneticVariation BEFREE The minor allele frequency for rs7903146 was different between TCP and FCPD patients carrying the N34S SPINK1 variant but did not reach statistical significance (OR = 1.59, 95% CI = 0.93-2.70, P = 0.09), while, TCF7L2variant showed a statistically significant association between TCP and FCPD patients carrying the 26V allele (OR = 1.69, 95% CI = 1.11-2.56, P = 0.013). 18706099 2008