Source: CURATED

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: rs1532085
rs1532085
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 6 2009 2013
dbSNP: rs1077834
rs1077834
15 58431280 intron variant T/C snv 0.34
High density lipoprotein measurement
0.700 1.000 5 2010 2019
dbSNP: rs1077835
rs1077835
15 58431227 intron variant A/G snv 0.34
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 5 2015 2019
dbSNP: rs261291
rs261291
1.000 0.080 15 58387979 intron variant T/A;C snv
High density lipoprotein measurement
0.700 1.000 5 2015 2019
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 3 2009 2012
dbSNP: rs13329672
rs13329672
15 58407738 intron variant C/T snv 0.31
High density lipoprotein measurement
0.700 1.000 3 2018 2019
dbSNP: rs2070895
rs2070895
0.807 0.120 15 58431740 intron variant G/A snv 0.33
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 3 2012 2012
dbSNP: rs4775041
rs4775041
1.000 0.040 15 58382496 intron variant G/C snv 0.24
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 3 2008 2012
dbSNP: rs4775041
rs4775041
1.000 0.040 15 58382496 intron variant G/C snv 0.24
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 3 2008 2013
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs1077834
rs1077834
15 58431280 intron variant T/C snv 0.34
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2018 2019
dbSNP: rs1077834
rs1077834
15 58431280 intron variant T/C snv 0.34
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2017 2018
dbSNP: rs1601935
rs1601935
15 58379566 intron variant G/T snv 0.60
High density lipoprotein measurement
0.700 1.000 2 2018 2019
dbSNP: rs1601935
rs1601935
15 58379566 intron variant G/T snv 0.60
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2015 2018
dbSNP: rs17821159
rs17821159
15 58264863 intron variant A/G snv 0.32
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs1800588
rs1800588
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2008 2012
dbSNP: rs2043085
rs2043085
0.827 0.080 15 58388755 intron variant T/C snv 0.54
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs261291
rs261291
1.000 0.080 15 58387979 intron variant T/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2018 2018
dbSNP: rs261334
rs261334
15 58434545 intron variant G/C snv 0.73
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs261342
rs261342
15 58438954 intron variant G/A;C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs473224
rs473224
15 58445142 intron variant T/A;G snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2009 2012
dbSNP: rs588136
rs588136
15 58438299 intron variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2012 2013
dbSNP: rs7350789
rs7350789
15 58387469 intron variant G/A snv 0.35
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2018 2018
dbSNP: rs7350789
rs7350789
15 58387469 intron variant G/A snv 0.35
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2018 2019
dbSNP: rs8034802
rs8034802
15 58432593 intron variant T/A snv 0.33
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2012 2012