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: rs3750601
rs3750601
10 98414804 non coding transcript exon variant C/A snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs6584204
rs6584204
10 98413823 intron variant C/G snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs7910247
rs7910247
10 98412495 intron variant C/T snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs7909131
rs7909131
10 98411714 non coding transcript exon variant A/G snv 0.49
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs10748729
rs10748729
10 98411614 non coding transcript exon variant G/C snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs3814142
rs3814142
10 98411347 non coding transcript exon variant C/G snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs3814141
rs3814141
10 98411271 non coding transcript exon variant G/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs3814140
rs3814140
10 98411005 intron variant C/T snv 0.34 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs7896828
rs7896828
10 98410750 non coding transcript exon variant A/T snv 0.49
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs6584202
rs6584202
10 98410626 non coding transcript exon variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs6584200
rs6584200
10 98410280 intron variant A/G snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs9804285
rs9804285
10 98409715 intron variant C/T snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs7923729
rs7923729
10 98409708 intron variant C/T snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs9787550
rs9787550
10 98409294 intron variant C/T snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs942803
rs942803
10 98408874 intron variant G/T snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs942804
rs942804
10 98408742 intron variant C/A snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs942805
rs942805
10 98408615 intron variant G/A snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs942806
rs942806
10 98408491 intron variant G/A snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs942807
rs942807
10 98408462 intron variant G/A snv 0.35
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs942808
rs942808
10 98408345 intron variant C/A snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs942809
rs942809
10 98408244 intron variant G/A snv 0.37
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs17109675
rs17109675
10 98408194 intron variant T/C snv 9.2E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs942810
rs942810
10 98408103 intron variant G/C snv 0.48
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs12763379
rs12763379
10 98407709 intron variant G/A snv 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs12763326
rs12763326
10 98407639 synonymous variant G/A snv 0.32 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013