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: rs12705932
rs12705932 		7 113987029 intron variant G/A snv 0.17
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2019 2019
dbSNP: rs71571192
rs71571192 		7 114030498 intron variant T/A snv 0.11
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1799999
rs1799999 		0.882 0.160 7 113878379 missense variant C/A snv 0.22 0.17
CUI: C1852091
Disease: INSULIN RESISTANCE, SUSCEPTIBILITY TO
INSULIN RESISTANCE, SUSCEPTIBILITY TO 		0.700 0
dbSNP: rs35449651
rs35449651 		1.000 0.080 7 113878300 missense variant G/T snv 1.4E-03 1.5E-03
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 0
dbSNP: rs1799999
rs1799999 		0.882 0.160 7 113878379 missense variant C/A snv 0.22 0.17
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.040 0.500 4 1998 2018
dbSNP: rs1799999
rs1799999 		0.882 0.160 7 113878379 missense variant C/A snv 0.22 0.17
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2002 2002
dbSNP: rs1799999
rs1799999 		0.882 0.160 7 113878379 missense variant C/A snv 0.22 0.17
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance 		Nutritional and Metabolic Diseases 0.010 < 0.001 1 2000 2000