AHSG, alpha 2-HS glycoprotein, 197

N. diseases: 204; N. variants: 18
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: rs4917
rs4917
0.790 0.160 3 186619924 missense variant T/C snv 0.68 0.68
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.020 1.000 2 2005 2015
dbSNP: rs4918
rs4918
0.763 0.400 3 186620593 missense variant G/A;C snv 0.67
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.020 1.000 2 2005 2016
dbSNP: rs2593813
rs2593813
1.000 0.080 3 186614782 intron variant G/A snv 0.63
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2005 2005
dbSNP: rs35457250
rs35457250
0.925 0.080 3 186620775 missense variant C/T snv 9.0E-03 8.1E-03
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2005 2005
dbSNP: rs573820635
rs573820635
1.000 0.080 3 186620844 missense variant C/T snv 2.1E-04 6.3E-05
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2005 2005