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: rs4775041
rs4775041
1.000 0.040 15 58382496 intron variant G/C snv 0.24
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 3 2008 2013
dbSNP: rs174455
rs174455
1.000 0.080 11 61888645 intron variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs174528
rs174528
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs174534
rs174534
1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs174541
rs174541
1.000 0.080 11 61798436 intron variant T/C snv 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs174545
rs174545
1.000 0.080 11 61801834 3 prime UTR variant C/A;G snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs174577
rs174577
1.000 0.080 11 61837342 intron variant C/A snv 0.38
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs174616
rs174616
1.000 0.080 11 61861650 intron variant G/A snv 0.51
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs2072114
rs2072114
1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs3733402
rs3733402
1.000 0.040 4 186236880 missense variant G/A;C snv 0.54
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2014
dbSNP: rs1000778
rs1000778
1.000 0.040 11 61887833 intron variant A/G snv 0.59
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs10096633
rs10096633
1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs10173355
rs10173355
1.000 2 233688675 intron variant A/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs102274
rs102274
1.000 0.080 11 61790354 non coding transcript exon variant T/C snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs10431386
rs10431386
1.000 0.040 12 120691123 intron variant C/T snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs10750097
rs10750097
1.000 0.040 11 116793324 upstream gene variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs10889332
rs10889332
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs11045879
rs11045879
1.000 0.120 12 21229685 intron variant T/C snv 0.18
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs11079035
rs11079035
1.000 0.040 17 42136994 intron variant G/A snv 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs11189600
rs11189600
1.000 0.040 10 98419517 intron variant C/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs1150253
rs1150253
1.000 0.080 1 206898250 intron variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs1150258
rs1150258
1.000 0.080 1 206901560 missense variant T/A;C;G snv 0.40 0.40
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs11668327
rs11668327
1.000 0.080 19 44895376 intron variant G/C snv 0.12
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs1168013
rs1168013
1.000 0.120 1 62531167 intron variant C/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs12042319
rs12042319
1.000 0.040 1 62584148 3 prime UTR variant G/A snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012