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: rs581080
rs581080 		9 15305380 intron variant G/C snv 0.72
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 5 2010 2019
dbSNP: rs581080
rs581080 		9 15305380 intron variant G/C snv 0.72
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 3 2010 2017
dbSNP: rs643531
rs643531 		9 15296036 intron variant C/A snv 0.89
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2010 2018
dbSNP: rs471364
rs471364 		1.000 0.040 9 15289580 intron variant C/T snv 0.87
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 1 2009 2009
dbSNP: rs540885
rs540885 		9 15294598 intron variant G/A;C;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2015 2018
dbSNP: rs581080
rs581080 		9 15305380 intron variant G/C snv 0.72
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2010 2013
dbSNP: rs686030
rs686030 		9 15304784 intron variant C/A snv 0.88
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2018 2019
dbSNP: rs117614852
rs117614852 		9 15279395 intron variant G/T snv 3.6E-03
CUI: C0562350
Disease: Hip circumference
Hip circumference 		0.700 1.000 1 2017 2017
dbSNP: rs1215112
rs1215112 		9 15303585 intron variant G/A snv 0.89
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1215112
rs1215112 		9 15303585 intron variant G/A snv 0.89
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs471364
rs471364 		1.000 0.040 9 15289580 intron variant C/T snv 0.87
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2009 2009
dbSNP: rs471364
rs471364 		1.000 0.040 9 15289580 intron variant C/T snv 0.87
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs486349
rs486349 		9 15293118 intron variant G/A;C snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs643531
rs643531 		9 15296036 intron variant C/A snv 0.89
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2010 2010
dbSNP: rs6474902
rs6474902 		9 15293948 intron variant C/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs675849
rs675849 		9 15298668 intron variant T/A;C;G snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs686030
rs686030 		9 15304784 intron variant C/A snv 0.88
CUI: C0242216
Disease: Biliary calculi
Biliary calculi 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs686030
rs686030 		9 15304784 intron variant C/A snv 0.88
CUI: C0016977
Disease: Gall Bladder Diseases
Gall Bladder Diseases 		Digestive System Diseases 0.010 1.000 1 2016 2016