Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17862866
rs17862866
2 233702266 intron variant A/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs17862875
rs17862875
2 233740656 intron variant G/A snv 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs17863787
rs17863787
0.925 0.040 2 233702448 intron variant T/G snv 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs17864701
rs17864701
2 233744071 intron variant C/T snv 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs1875263
rs1875263
1.000 2 233716976 intron variant C/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs1983023
rs1983023
2 233728376 intron variant T/C snv 0.46
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs2008595
rs2008595
2 233728546 intron variant C/T snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs2018985
rs2018985
2 233740214 intron variant A/G snv 0.47
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs2070959
rs2070959
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs28899170
rs28899170
2 233695584 intron variant C/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs3755319
rs3755319
0.925 0.120 2 233758936 intron variant A/C;G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs3771341
rs3771341
2 233764593 intron variant G/A;T snv 0.33
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs3806596
rs3806596
2 233729061 intron variant T/C snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs3806597
rs3806597
2 233728923 intron variant A/G snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs4124874
rs4124874
0.851 0.120 2 233757013 intron variant T/A;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs4148324
rs4148324
2 233764076 intron variant T/A;G snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs4148325
rs4148325
0.851 0.080 2 233764663 intron variant C/T snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs4148326
rs4148326
0.925 0.080 2 233764816 intron variant T/C snv 0.49
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs4261716
rs4261716
2 233684471 intron variant G/T snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs4294999
rs4294999
2 233726821 intron variant A/G snv 0.54
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs4347832
rs4347832
2 233684395 intron variant T/C snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs4399719
rs4399719
2 233757815 intron variant T/G snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs4530361
rs4530361
2 233681395 intron variant A/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs4553819
rs4553819
2 233685437 intron variant A/G snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs4663333
rs4663333
2 233746657 intron variant G/T snv 0.55
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013