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: rs1082214
rs1082214
0.925 0.080 12 56452706 non coding transcript exon variant C/T snv 9.3E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs12313841
rs12313841
12 56462834 intron variant C/T snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2638318
rs2638318
12 56463638 intron variant C/T snv 0.55
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2638319
rs2638319
12 56463273 intron variant C/T snv 0.55
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs34287864
rs34287864
12 56464533 intron variant G/A snv 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs7302925
rs7302925
12 56467674 intron variant A/G snv 0.69
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs799187
rs799187
12 56452059 intron variant T/A snv 1.0E-01
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012