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: rs10119043
rs10119043
9 135122706 downstream gene variant C/T snv 0.11
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs116965780
rs116965780
18 43300829 intergenic variant C/T snv 7.0E-02
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs1461494
rs1461494
11 123055777 downstream gene variant T/A;C snv
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs1836778
rs1836778
4 29332870 intergenic variant T/C snv 0.56
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs1966678
rs1966678
4 29322410 intergenic variant T/G snv 0.60
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs2226150
rs2226150
6 77349634 intergenic variant G/A snv 0.49
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs4435343
rs4435343
18 43322011 intergenic variant C/A;T snv
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs4936767
rs4936767
11 123047451 upstream gene variant A/G snv 0.34
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs55920741
rs55920741
4 29331415 intergenic variant C/T snv 0.39
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs57580384
rs57580384
8 26048063 upstream gene variant G/A snv 0.14
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs59926619
rs59926619
8 26050704 intergenic variant G/A snv 0.13
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs638436
rs638436
11 56495636 upstream gene variant G/A snv 0.58
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs638452
rs638452
11 56495642 upstream gene variant A/T snv 0.58
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs6448638
rs6448638
4 29333941 intergenic variant T/C snv 0.56
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs72609945
rs72609945
8 26048781 upstream gene variant C/A;T snv 0.13
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs72749479
rs72749479
9 80667356 intergenic variant T/C snv 8.5E-02
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs72749483
rs72749483
9 80670259 intergenic variant T/C snv 8.5E-02
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs79666748
rs79666748
18 43280443 upstream gene variant A/C snv 7.0E-02
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs9341664
rs9341664
6 77375469 intergenic variant A/C snv 0.51
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs17079585
rs17079585
13 23921903 regulatory region variant G/A snv 1.9E-02
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2017 2017
dbSNP: rs10041590
rs10041590
5 24064827 intron variant T/C;G snv
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs10054178
rs10054178
5 24059742 intron variant A/G snv 7.5E-02
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs10056373
rs10056373
5 24069684 intron variant C/T snv 7.4E-02
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs113051092
rs113051092
5 24060490 intron variant A/T snv 7.4E-02
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs16893073
rs16893073
5 24072508 intron variant C/G;T snv
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015