Source: GWASCAT

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: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.890 0.900 2 2010 2019
dbSNP: rs493258
rs493258
0.925 0.040 15 58395681 intron variant T/C snv 0.50
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.860 1.000 1 2010 2019
dbSNP: rs3784262
rs3784262
0.882 0.160 15 57960908 intron variant T/A;C snv
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus
0.820 0.667 1 2013 2016
dbSNP: rs920915
rs920915
1.000 0.040 15 58396268 intron variant C/G snv 0.55
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.810 1.000 1 2013 2019
dbSNP: rs1532085
rs1532085
0.882 0.080 15 58391167 intron variant A/G;T snv
High density lipoprotein measurement
0.800 1.000 8 2009 2019
dbSNP: rs1800588
rs1800588
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 5 2012 2019
dbSNP: rs261334
rs261334
15 58434545 intron variant G/C snv 0.73
High density lipoprotein measurement
0.800 1.000 5 2010 2019
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
High density lipoprotein measurement
0.800 1.000 4 2009 2019
dbSNP: rs1532085
rs1532085
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 4 2010 2019
dbSNP: rs1532085
rs1532085
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2009 2018
dbSNP: rs1800588
rs1800588
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30
High density lipoprotein measurement
0.800 1.000 4 2008 2019
dbSNP: rs2070895
rs2070895
0.807 0.120 15 58431740 intron variant G/A snv 0.33
High density lipoprotein measurement
0.800 1.000 4 2012 2019
dbSNP: rs1077835
rs1077835
15 58431227 intron variant A/G snv 0.34
High density lipoprotein measurement
0.800 1.000 3 2013 2019
dbSNP: rs16940212
rs16940212
1.000 0.040 15 58401821 intron variant G/A;T snv
High density lipoprotein measurement
0.800 1.000 3 2011 2019
dbSNP: rs1800588
rs1800588
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 3 2012 2018
dbSNP: rs4775041
rs4775041
1.000 0.040 15 58382496 intron variant G/C snv 0.24
High density lipoprotein measurement
0.800 1.000 3 2008 2019
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2012 2018
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
High density lipoprotein measurement
0.800 1.000 2 2012 2018
dbSNP: rs261342
rs261342
15 58438954 intron variant G/A;C;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2012 2019
dbSNP: rs261342
rs261342
15 58438954 intron variant G/A;C;T snv
High density lipoprotein measurement
0.800 1.000 2 2012 2019
dbSNP: rs4775041
rs4775041
1.000 0.040 15 58382496 intron variant G/C snv 0.24
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2008 2018
dbSNP: rs8034802
rs8034802
15 58432593 intron variant T/A snv 0.33
High density lipoprotein measurement
0.800 1.000 2 2011 2019
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2009 2018
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1.000 1 2011 2011
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012