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: rs3826796
rs3826796 		19 46296578 upstream gene variant G/T snv 7.7E-02
CUI: C0523560
Disease: VLDL cholesterol measurement
VLDL cholesterol measurement 		0.700 1.000 1 2017 2017
dbSNP: rs3826796
rs3826796 		19 46296578 upstream gene variant G/T snv 7.7E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2017 2017
dbSNP: rs3826795
rs3826795 		0.925 0.120 19 46297176 intron variant G/A;T snv
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3826795
rs3826795 		0.925 0.120 19 46297176 intron variant G/A;T snv
CUI: C1266129
Disease: Atypical Lipoma
Atypical Lipoma 		Neoplasms 0.010 < 0.001 1 2017 2017