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: rs11053550
rs11053550
12 10019754 intron variant T/C snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs893245
rs893245
2 100198431 regulatory region variant C/T snv 0.55
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs6542920
rs6542920
2 100228626 intron variant A/G snv 0.64
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs4851273
rs4851273
2 100231859 intron variant A/G snv 0.64
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs4437940
rs4437940
10 10023280 intergenic variant G/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs7597861
rs7597861
2 100236725 intron variant G/A snv 0.65
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs12474386
rs12474386
2 100240555 intron variant G/A snv 0.46
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs6739695
rs6739695
2 100243160 intron variant A/C;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs10865036
rs10865036
2 100244133 intron variant T/C snv 0.65
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2309811
rs2309811
2 100245897 intron variant A/G snv 0.65
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs6737502
rs6737502
2 100246441 intron variant C/T snv 0.65
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs6542921
rs6542921
2 100248036 intron variant C/A snv 0.64
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs4851274
rs4851274
2 100254400 downstream gene variant T/C snv 0.65
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs603424
rs603424
1.000 0.080 10 100315722 intron variant G/A snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2014 2014
dbSNP: rs10783130
rs10783130
1 100341341 upstream gene variant C/G snv 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs11166439
rs11166439
1 100342730 upstream gene variant G/C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs537783
rs537783
11 100377590 intergenic variant C/A snv 0.16
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs1145412
rs1145412
11 100378042 intergenic variant T/C snv 0.17
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs10894847
rs10894847
11 100385044 intergenic variant G/T snv 0.17
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs9386144
rs9386144
6 100425381 intron variant T/C snv 0.17
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs3778033
rs3778033
6 100427640 intron variant T/C snv 0.19
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs12769144
rs12769144
10 101609797 downstream gene variant A/C snv 7.6E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs985375
rs985375
3 102348402 intron variant G/A snv 0.31
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs10820660
rs10820660
9 104503209 upstream gene variant A/G snv 0.13
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs17812021
rs17812021
12 104534885 intron variant C/G snv 5.0E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013