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: rs439401
rs439401 		0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 5 2009 2019
dbSNP: rs562338
rs562338 		0.807 0.160 2 21065449 intergenic variant A/G snv 0.69
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 5 2008 2019
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: rs6920220
rs6920220 		0.742 0.440 6 137685367 intron variant G/A snv 0.16
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.900 0.938 5 2007 2019
dbSNP: rs8099917
rs8099917 		0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic 		0.900 1.000 5 2009 2019
dbSNP: rs10503669
rs10503669 		0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 4 2008 2019
dbSNP: rs10503669
rs10503669 		0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 4 2008 2012
dbSNP: rs12068753
rs12068753 		1.000 0.120 1 159722747 intergenic variant T/A snv 0.15
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.800 1.000 4 2012 2015
dbSNP: rs12143842
rs12143842 		0.925 0.160 1 162064100 intergenic variant C/T snv 0.22
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 4 2009 2019
dbSNP: rs1387153
rs1387153 		0.807 0.200 11 92940662 downstream gene variant C/G;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.880 1.000 4 2009 2019
dbSNP: rs1394371
rs1394371 		0.925 0.080 15 78432127 intergenic variant C/T snv 0.22
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.700 1.000 4 2008 2012
dbSNP: rs17693963
rs17693963 		0.882 0.040 6 27742386 upstream gene variant A/C;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 1.000 4 2009 2014
dbSNP: rs2027471
rs2027471 		1 159719598 intergenic variant T/A snv 0.32
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 4 2012 2014
dbSNP: rs2395173
rs2395173 		0.882 0.240 6 32437082 upstream gene variant A/G snv 0.62
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 4 2007 2011
dbSNP: rs2542151
rs2542151 		0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.880 1.000 4 2007 2016
dbSNP: rs2808628
rs2808628 		1 159706221 upstream gene variant G/A snv 0.31
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 4 2012 2014
dbSNP: rs2808629
rs2808629 		0.925 0.160 1 159707006 upstream gene variant G/A snv 0.31
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 4 2012 2014
dbSNP: rs2954029
rs2954029 		0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 4 2010 2019
dbSNP: rs2954029
rs2954029 		0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 4 2010 2013
dbSNP: rs2954029
rs2954029 		0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 4 2010 2019
dbSNP: rs2954029
rs2954029 		0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 4 2010 2019
dbSNP: rs2954029
rs2954029 		0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 4 2010 2013
dbSNP: rs2965101
rs2965101 		1.000 0.080 19 44734556 intergenic variant T/C snv 0.34
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 4 2009 2012
dbSNP: rs3764261
rs3764261 		0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 4 2010 2019
dbSNP: rs3764261
rs3764261 		0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 4 2009 2018