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: rs7122226
rs7122226 		11 119081014 intron variant A/G snv 4.2E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7122226
rs7122226 		11 119081014 intron variant A/G snv 4.2E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34757931
rs34757931 		0.742 0.360 11 119081189 missense variant T/G snv 1.2E-04 5.6E-05
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy 		Nervous System Diseases 0.710 1.000 1 2016 2016
dbSNP: rs1185460
rs1185460 		1.000 0.040 11 119072723 non coding transcript exon variant A/G snv 0.48
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs15818
rs15818 		11 119081463 missense variant A/G snv 0.36 0.40
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2018 2018
dbSNP: rs3825061
rs3825061 		11 119073965 intron variant C/T snv 0.33 0.33
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs3825061
rs3825061 		11 119073965 intron variant C/T snv 0.33 0.33
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs7925100
rs7925100 		11 119070886 intron variant G/A snv 0.33
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019