CTRB2, chymotrypsinogen B2, 440387

N. diseases: 5; N. variants: 4
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs8051363
rs8051363 		16 75221319 intron variant A/G snv 0.76
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 2 2018 2018
dbSNP: rs8055167
rs8055167 		1.000 0.080 16 75220991 intron variant T/C snv 0.71
CUI: C0376670
Disease: Pancreatitis, Alcoholic
Pancreatitis, Alcoholic 		Digestive System Diseases; Chemically-Induced Disorders 0.700 1.000 1 2018 2018
dbSNP: rs889512
rs889512 		16 75208114 upstream gene variant C/G snv 0.10
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs9928842
rs9928842 		1.000 0.080 16 75208969 upstream gene variant T/C;G snv
CUI: C0376670
Disease: Pancreatitis, Alcoholic
Pancreatitis, Alcoholic 		Digestive System Diseases; Chemically-Induced Disorders 0.700 1.000 1 2018 2018