APOA5, apolipoprotein A5, 116519

N. diseases: 107; N. variants: 22
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: rs651821
rs651821 		0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 9 2012 2019
dbSNP: rs662799
rs662799 		0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 8 2012 2019
dbSNP: rs662799
rs662799 		0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 7 2012 2019
dbSNP: rs651821
rs651821 		0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 5 2012 2019
dbSNP: rs9804646
rs9804646 		11 116794363 upstream gene variant C/T snv 0.17
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 5 2012 2019
dbSNP: rs3135506
rs3135506 		0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 4 2009 2019
dbSNP: rs651821
rs651821 		0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 4 2012 2019
dbSNP: rs2075291
rs2075291 		0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 3 2018 2019
dbSNP: rs2075291
rs2075291 		0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 3 2018 2019
dbSNP: rs2266788
rs2266788 		0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2011 2018
dbSNP: rs2266788
rs2266788 		0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 3 2011 2018
dbSNP: rs3135506
rs3135506 		0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 3 2018 2019
dbSNP: rs662799
rs662799 		0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 3 2012 2019
dbSNP: rs10750097
rs10750097 		1.000 0.040 11 116793324 upstream gene variant G/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2012 2012
dbSNP: rs10750097
rs10750097 		1.000 0.040 11 116793324 upstream gene variant G/A;C snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs10750097
rs10750097 		1.000 0.040 11 116793324 upstream gene variant G/A;C snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2012 2012
dbSNP: rs12287066
rs12287066 		11 116791615 synonymous variant G/T snv 7.7E-02 0.10
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2012 2012
dbSNP: rs2266788
rs2266788 		0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 2 2012 2018
dbSNP: rs3135506
rs3135506 		0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2018 2019
dbSNP: rs662799
rs662799 		0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs9804646
rs9804646 		11 116794363 upstream gene variant C/T snv 0.17
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 2 2012 2018
dbSNP: rs10750097
rs10750097 		1.000 0.040 11 116793324 upstream gene variant G/A;C snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10750097
rs10750097 		1.000 0.040 11 116793324 upstream gene variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12287066
rs12287066 		11 116791615 synonymous variant G/T snv 7.7E-02 0.10
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12287066
rs12287066 		11 116791615 synonymous variant G/T snv 7.7E-02 0.10
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012