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: rs11869286
rs11869286 		0.925 0.080 17 39657603 intron variant G/C snv 0.52
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 4 2010 2019
dbSNP: rs11869286
rs11869286 		0.925 0.080 17 39657603 intron variant G/C snv 0.52
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2010 2013
dbSNP: rs2271308
rs2271308 		1.000 0.080 17 39661229 non coding transcript exon variant T/C snv 0.61
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 2 2010 2011
dbSNP: rs881844
rs881844 		0.925 0.080 17 39653965 intron variant C/G snv 0.51
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2018 2019
dbSNP: rs147005258
rs147005258 		17 39644735 intron variant C/G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs1877031
rs1877031 		0.827 0.280 17 39657827 missense variant G/A snv 0.62 0.52
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2010 2010
dbSNP: rs1877031
rs1877031 		0.827 0.280 17 39657827 missense variant G/A snv 0.62 0.52
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2017 2017
dbSNP: rs72827176
rs72827176 		1.000 0.080 17 39654542 intron variant C/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs881844
rs881844 		0.925 0.080 17 39653965 intron variant C/G snv 0.51
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs9972882
rs9972882 		0.925 0.080 17 39651445 intron variant A/C snv 0.66
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs9972882
rs9972882 		0.925 0.080 17 39651445 intron variant A/C snv 0.66
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11869286
rs11869286 		0.925 0.080 17 39657603 intron variant G/C snv 0.52
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs11869286
rs11869286 		0.925 0.080 17 39657603 intron variant G/C snv 0.52
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs1877031
rs1877031 		0.827 0.280 17 39657827 missense variant G/A snv 0.62 0.52
CUI: C0206696
Disease: Carcinoma, Signet Ring Cell
Carcinoma, Signet Ring Cell 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs1877031
rs1877031 		0.827 0.280 17 39657827 missense variant G/A snv 0.62 0.52
CUI: C1691215
Disease: Penile hypospadias
Penile hypospadias 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1877031
rs1877031 		0.827 0.280 17 39657827 missense variant G/A snv 0.62 0.52
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs1877031
rs1877031 		0.827 0.280 17 39657827 missense variant G/A snv 0.62 0.52
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs881844
rs881844 		0.925 0.080 17 39653965 intron variant C/G snv 0.51
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs881844
rs881844 		0.925 0.080 17 39653965 intron variant C/G snv 0.51
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs9972882
rs9972882 		0.925 0.080 17 39651445 intron variant A/C snv 0.66
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs9972882
rs9972882 		0.925 0.080 17 39651445 intron variant A/C snv 0.66
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014