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: rs61394862
rs61394862
1.000 0.040 5 14850985 intron variant C/G;T snv
CUI: C0017601
Disease: Glaucoma
Glaucoma
Eye Diseases 0.700 1.000 1 2018 2018
dbSNP: rs6885132
rs6885132
1.000 0.080 5 14767983 intron variant C/G;T snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs76325372
rs76325372
1.000 0.040 5 14837223 intron variant A/C;T snv
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
Eye Diseases 0.700 1.000 1 2018 2018
dbSNP: rs875525
rs875525
0.925 0.080 5 14747138 intron variant C/T snv 0.36
CUI: C0033802
Disease: Pseudogout
Pseudogout
Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.010 1.000 1 2014 2014
dbSNP: rs875525
rs875525
0.925 0.080 5 14747138 intron variant C/T snv 0.36
Calcium pyrophosphate deposition disease
Musculoskeletal Diseases 0.010 1.000 1 2014 2014