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: rs1042034
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 3 2010 2019
dbSNP: rs1042034
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2010 2019
dbSNP: rs1042034
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2010 2012
dbSNP: rs1042034
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1042034
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 1 2012 2018
dbSNP: rs1042034
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1042034
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 1 2012 2018
dbSNP: rs1042031
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1042031
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1042031
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2678379
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 1 2012 2019
dbSNP: rs2678379
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 1 2012 2019
dbSNP: rs2678379
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2678379
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 1 2012 2018
dbSNP: rs2678379
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 1 2012 2018
dbSNP: rs2678379
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2678379
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1800479
rs1800479
APOB
2 21004511 intron variant C/G snv 0.16 0.17
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1800479
rs1800479
APOB
2 21004511 intron variant C/G snv 0.16 0.17
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1800479
rs1800479
APOB
2 21004511 intron variant C/G snv 0.16 0.17
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5742904
rs5742904
APOB
0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs5742904
rs5742904
APOB
0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 2 2012 2014
dbSNP: rs5742904
rs5742904
APOB
0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total 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: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 2 2012 2018
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