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: rs8179252
rs8179252
0.882 0.120 2 27523965 downstream gene variant A/C snv 0.37
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 1 2013 2013
dbSNP: rs8179252
rs8179252
0.882 0.120 2 27523965 downstream gene variant A/C snv 0.37
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 1 2013 2013
dbSNP: rs704790
rs704790
2 27523543 3 prime UTR variant G/A snv 4.0E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs11681351
rs11681351
0.925 0.120 2 27520556 intron variant G/A snv 0.36
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 2 2010 2013
dbSNP: rs11681351
rs11681351
0.925 0.120 2 27520556 intron variant G/A snv 0.36
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 2 2010 2013
dbSNP: rs11681351
rs11681351
0.925 0.120 2 27520556 intron variant G/A snv 0.36
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs814295
rs814295
0.925 0.120 2 27520348 intron variant A/G snv 0.18
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 1 2013 2013
dbSNP: rs814295
rs814295
0.925 0.120 2 27520348 intron variant A/G snv 0.18
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs814295
rs814295
0.925 0.120 2 27520348 intron variant A/G snv 0.18
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs814295
rs814295
0.925 0.120 2 27520348 intron variant A/G snv 0.18
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 1 2013 2013
dbSNP: rs814295
rs814295
0.925 0.120 2 27520348 intron variant A/G snv 0.18
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2012 2017
dbSNP: rs780092
rs780092
0.827 0.160 2 27520287 intron variant A/G snv 0.18
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.800 1.000 2 2011 2012
dbSNP: rs780092
rs780092
0.827 0.160 2 27520287 intron variant A/G snv 0.18
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 1 2013 2013
dbSNP: rs780092
rs780092
0.827 0.160 2 27520287 intron variant A/G snv 0.18
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2013 2017
dbSNP: rs780092
rs780092
0.827 0.160 2 27520287 intron variant A/G snv 0.18
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2011 2019
dbSNP: rs780092
rs780092
0.827 0.160 2 27520287 intron variant A/G snv 0.18
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 1 2013 2013
dbSNP: rs780093
rs780093
0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 3 2010 2013
dbSNP: rs780093
rs780093
0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 3 2010 2013
dbSNP: rs780093
rs780093
0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2011 2019
dbSNP: rs780093
rs780093
0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 2 2011 2013
dbSNP: rs780093
rs780093
0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2010 2010
dbSNP: rs780093
rs780093
0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C0919677
Disease: Protein C measurement
Protein C measurement
0.700 1.000 1 2010 2010
dbSNP: rs780093
rs780093
0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2012 2019
dbSNP: rs780093
rs780093
0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C0337434
Disease: Estradiol measurement
Estradiol measurement
0.700 1.000 1 2012 2012
dbSNP: rs780093
rs780093
0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012