Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs673548
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2012 2019
dbSNP: rs673548
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2009 2019
dbSNP: rs673548
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs676210
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 2 2012 2018
dbSNP: rs597331
rs597331
APOB
2 21039555 intron variant G/A;T snv
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs597331
rs597331
APOB
2 21039555 intron variant G/A;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs597331
rs597331
APOB
2 21039555 intron variant G/A;T snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs673548
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 1 2012 2018
dbSNP: rs673548
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2009 2009
dbSNP: rs673548
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs673548
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2009 2009
dbSNP: rs673548
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 1 2012 2018
dbSNP: rs673548
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs673548
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2012 2012
dbSNP: rs676210
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 1 2012 2018
dbSNP: rs676210
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 1 2012 2019
dbSNP: rs676210
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs676210
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs676210
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs676210
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 1 2012 2019
dbSNP: rs12720847
rs12720847
APOB
2 21012503 missense variant G/A;C snv 5.1E-03
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs693
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 5 2008 2012
dbSNP: rs693
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 5 2007 2019
dbSNP: rs1367117
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 3 2010 2019
dbSNP: rs1367117
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 3 2010 2013