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: rs12972970
rs12972970
19 44884339 intron variant G/A snv 0.10
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs1871047
rs1871047
1.000 0.080 19 44848489 intron variant A/G snv 0.31
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
0.700 1.000 1 2009 2009
dbSNP: rs2075642
rs2075642
19 44874210 intron variant G/A;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2075642
rs2075642
19 44874210 intron variant G/A;T snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2075642
rs2075642
19 44874210 intron variant G/A;T snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs283813
rs283813
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2009 2009
dbSNP: rs283813
rs283813
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011
dbSNP: rs283813
rs283813
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs34342646
rs34342646
19 44884873 intron variant G/A snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs365653
rs365653
1.000 0.080 19 44858389 intron variant A/G snv 0.16
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs377702
rs377702
1.000 0.080 19 44859410 intron variant G/A snv 0.34
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
0.700 1.000 1 2009 2009
dbSNP: rs3852856
rs3852856
19 44858317 intron variant G/A;C;T snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs3852856
rs3852856
19 44858317 intron variant G/A;C;T snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs3852856
rs3852856
19 44858317 intron variant G/A;C;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs387976
rs387976
1.000 0.080 19 44875803 intron variant A/C;T snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs387976
rs387976
1.000 0.080 19 44875803 intron variant A/C;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs387976
rs387976
1.000 0.080 19 44875803 intron variant A/C;T snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs387976
rs387976
1.000 0.080 19 44875803 intron variant A/C;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2011 2011
dbSNP: rs416041
rs416041
1.000 0.080 19 44867597 intron variant G/A;C snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2011 2011
dbSNP: rs4803763
rs4803763
1.000 0.080 19 44854034 intron variant G/A;C snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs4803763
rs4803763
1.000 0.080 19 44854034 intron variant G/A;C snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs4803763
rs4803763
1.000 0.080 19 44854034 intron variant G/A;C snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs4803766
rs4803766
19 44867911 intron variant G/A snv 0.44
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs4803766
rs4803766
19 44867911 intron variant G/A snv 0.44
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs519113
rs519113
1.000 0.080 19 44873027 intron variant C/G;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2011 2011