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: rs10735864
rs10735864
12 56538519 intron variant A/C;G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2657899
rs2657899
12 56537619 intron variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2657901
rs2657901
12 56539632 intron variant A/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2657902
rs2657902
12 56539867 intron variant G/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2657903
rs2657903
12 56539938 intron variant G/A;C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs4759253
rs4759253
12 56584387 intron variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs7299189
rs7299189
12 56579072 intron variant C/A;G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs7307755
rs7307755
12 56581001 intron variant A/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs799261
rs799261
12 56530605 intron variant C/A;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs116287412
rs116287412
12 56552231 intron variant T/C snv 6.9E-03
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2638301
rs2638301
12 56535030 intron variant A/G snv 0.10
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs7977500
rs7977500
12 56575497 intron variant C/G snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2950391
rs2950391
12 56579359 intron variant G/A snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2694919
rs2694919
12 56523606 intron variant C/T snv 0.12
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs774211
rs774211
12 56527155 intron variant T/C snv 0.12
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs774211
rs774211
12 56527155 intron variant T/C snv 0.12
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs774211
rs774211
12 56527155 intron variant T/C snv 0.12
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement
0.700 1.000 1 2019 2019
dbSNP: rs774211
rs774211
12 56527155 intron variant T/C snv 0.12
CUI: C0302274
Disease: Glutamine measurement
Glutamine measurement
0.700 1.000 1 2019 2019
dbSNP: rs813497
rs813497
12 56530332 intron variant G/A snv 0.12
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2657896
rs2657896
12 56535910 intron variant C/T snv 0.12
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs12232026
rs12232026
12 56566982 intron variant T/A snv 0.14
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2694917
rs2694917
12 56519080 upstream gene variant T/C snv 0.17
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2950389
rs2950389
12 56591774 3 prime UTR variant C/A snv 0.19
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2018 2018
dbSNP: rs36073309
rs36073309
12 56537208 intron variant G/A snv 0.32
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs7312441
rs7312441
12 56547362 intron variant C/A snv 0.33
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012