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: rs4420638
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 10 2008 2013
dbSNP: rs6511720
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 10 2008 2013
dbSNP: rs3764261
rs3764261 		0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 8 2008 2013
dbSNP: rs11206510
rs11206510 		0.763 0.240 1 55030366 intergenic variant T/A;C;G snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 6 2008 2013
dbSNP: rs1532085
rs1532085
ALDH1A2
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: rs4242384
rs4242384 		0.882 0.160 8 127506309 regulatory region variant C/A snv 0.88
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.700 1.000 6 2008 2013
dbSNP: rs646776
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 6 2008 2013
dbSNP: rs964184
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 6 2009 2013
dbSNP: rs9989419
rs9989419 		0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 6 2008 2014
dbSNP: rs10401969
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 5 2009 2013
dbSNP: rs10938397
rs10938397 		0.851 0.200 4 45180510 intergenic variant A/G snv 0.37
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 5 2009 2013
dbSNP: rs10938397
rs10938397 		0.851 0.200 4 45180510 intergenic variant A/G snv 0.37
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 5 2009 2013
dbSNP: rs1205
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 5 2012 2014
dbSNP: rs12678919
rs12678919 		0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 5 2009 2013
dbSNP: rs12740374
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 5 2008 2012
dbSNP: rs12916
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 5 2010 2013
dbSNP: rs1558902
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 5 2010 2014
dbSNP: rs1558902
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 5 2010 2014
dbSNP: rs1800775
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 5 2008 2013
dbSNP: rs1883025
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 5 2009 2013
dbSNP: rs3755319
rs3755319
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A5 ; UGT1A9 ; UGT1A4 ; UGT1A1 ; UGT1A3
0.925 0.120 2 233758936 intron variant A/C;G;T snv
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		0.700 1.000 5 2009 2013
dbSNP: rs417968
rs417968
LINC02210 ; LINC02210-CRHR1
1.000 0.040 17 45651010 non coding transcript exon variant G/A snv 0.65
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 5 2009 2014
dbSNP: rs4846914
rs4846914
GALNT2
0.925 0.080 1 230159944 intron variant G/A snv 0.45
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 5 2008 2013
dbSNP: rs562338
rs562338 		0.807 0.160 2 21065449 intergenic variant A/G snv 0.69
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 5 2008 2012
dbSNP: rs599839
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 5 2008 2013