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
High density lipoprotein measurement
0.800 1.000 4 2009 2019
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: 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
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs1077834
rs1077834
15 58431280 intron variant T/C snv 0.34
High density lipoprotein measurement
0.700 1.000 5 2010 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: 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: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2016 2016
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: rs1077835
rs1077835
15 58431227 intron variant A/G snv 0.34
High density lipoprotein measurement
0.800 1.000 3 2013 2019
dbSNP: rs1077835
rs1077835
15 58431227 intron variant A/G snv 0.34
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs11631342
rs11631342
1.000 0.040 15 58432184 non coding transcript exon variant A/G snv 5.6E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.700 1.000 1 2018 2018
dbSNP: rs118146059
rs118146059
15 58252574 intron variant T/C snv 1.7E-03
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs12148399
rs12148399
15 58289171 intron variant T/A snv 0.14
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs12148399
rs12148399
15 58289171 intron variant T/A snv 0.14
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs12148780
rs12148780
1.000 0.080 15 58289090 intron variant A/G snv 0.14
High density lipoprotein measurement
0.700 1.000 1 2019 2019
dbSNP: rs12148780
rs12148780
1.000 0.080 15 58289090 intron variant A/G snv 0.14
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2019 2019
dbSNP: rs12903590
rs12903590
15 58285578 intron variant A/T snv 0.15
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs12914626
rs12914626
1.000 0.040 15 58446224 intron variant C/T snv 0.54
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2015 2015
dbSNP: rs13329672
rs13329672
15 58407738 intron variant C/T snv 0.31
High density lipoprotein measurement
0.700 1.000 3 2018 2019
dbSNP: rs13329672
rs13329672
15 58407738 intron variant C/T snv 0.31
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs13329672
rs13329672
15 58407738 intron variant C/T snv 0.31
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
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