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: rs10517480
rs10517480
4 59883111 intergenic variant A/T snv 0.27
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2008 2008
dbSNP: rs10953730
rs10953730
7 113271355 intergenic variant A/C;G snv 0.25
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2008 2008
dbSNP: rs1148259
rs1148259
10 37219522 synonymous variant A/C snv 0.50 0.44
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2008 2008
dbSNP: rs1382269
rs1382269
3 137389640 intergenic variant T/C snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2008 2008
dbSNP: rs1591830
rs1591830
6 150330764 upstream gene variant G/A snv 0.48
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2008 2008
dbSNP: rs17267292
rs17267292
13 92670893 intron variant T/C snv 0.22
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2008 2008
dbSNP: rs2194980
rs2194980
12 115064913 intergenic variant A/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2008 2008
dbSNP: rs2900976
rs2900976
2 71731350 intergenic variant C/T snv 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2008 2008
dbSNP: rs4453795
rs4453795
3 192376186 intron variant A/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2008 2008
dbSNP: rs6807064
rs6807064
3 10494087 intron variant C/T snv 0.35
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2008 2008
dbSNP: rs886144
rs886144
15 91174122 intron variant C/T snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2008 2008
dbSNP: rs9309413
rs9309413
2 68343640 intergenic variant G/A;C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2008 2008
dbSNP: rs9354308
rs9354308
6 65855460 intergenic variant G/A snv 0.65
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2008 2008
dbSNP: rs992037
rs992037
6 161580404 intron variant T/C snv 0.71
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2008 2008
dbSNP: rs9924951
rs9924951
16 7454852 intron variant G/A snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2008 2008
dbSNP: rs211718
rs211718
1 75640990 downstream gene variant T/C snv 0.75
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2010 2010
dbSNP: rs8396
rs8396
4 158709665 3 prime UTR variant T/C snv 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2010 2010
dbSNP: rs10830962
rs10830962
0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2011 2011
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2011 2011
dbSNP: rs12483959
rs12483959
1.000 22 43930116 intron variant G/A;C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2011 2011
dbSNP: rs12654264
rs12654264
0.925 0.120 5 75352778 intron variant A/T snv 0.38
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2011 2011
dbSNP: rs13069049
rs13069049
3 66759518 intergenic variant A/T snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2011 2011
dbSNP: rs16856247
rs16856247
2 168927903 intron variant C/T snv 6.6E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2011 2011
dbSNP: rs1799884
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2011 2011
dbSNP: rs2738446
rs2738446
19 11116650 intron variant C/A;G snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2011 2011