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: rs12683159
rs12683159
9 131723496 intron variant G/A;C snv 0.36
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs11243444
rs11243444
1.000 0.080 9 131597867 intron variant T/C;G snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 1.000 2 2009 2011
dbSNP: rs7853122
rs7853122
0.925 0.080 9 131705224 intron variant C/T snv 0.87
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs7853122
rs7853122
0.925 0.080 9 131705224 intron variant C/T snv 0.87
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs7853122
rs7853122
0.925 0.080 9 131705224 intron variant C/T snv 0.87
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2011 2011