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: 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: rs10152202
rs10152202
15 58452149 intron variant T/G snv 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs10518976
rs10518976
15 58459002 intron variant T/A snv 7.6E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs11858164
rs11858164
15 58450532 intron variant T/G snv 0.39
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2008 2008
dbSNP: rs11858164
rs11858164
15 58450532 intron variant T/G snv 0.39
High density lipoprotein measurement
0.700 1.000 1 2008 2008
dbSNP: rs11858164
rs11858164
15 58450532 intron variant T/G snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs12900622
rs12900622
15 58439256 intron variant T/C snv 0.10
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs12914035
rs12914035
15 58438690 intron variant A/G snv 0.10
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs12914626
rs12914626
1.000 0.040 15 58446224 intron variant C/T snv 0.54
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs17190517
rs17190517
15 58436945 intron variant C/T snv 0.37 0.33
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs17190517
rs17190517
15 58436945 intron variant C/T snv 0.37 0.33
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs17190517
rs17190517
15 58436945 intron variant C/T snv 0.37 0.33
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs17269264
rs17269264
15 58446561 intron variant G/A snv 0.37
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs17269264
rs17269264
15 58446561 intron variant G/A snv 0.37
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs17269264
rs17269264
15 58446561 intron variant G/A snv 0.37
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs17269271
rs17269271
15 58447562 intron variant G/C snv 0.38
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs17269271
rs17269271
15 58447562 intron variant G/C snv 0.38
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs17269271
rs17269271
15 58447562 intron variant G/C snv 0.38
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2012 2016
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2008 2008
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 1 2012 2018