Disease: Creatinine clearance measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10119043 9 135122706 downstream gene variant C/T snv 0.11 2
rs116965780 18 43300829 intergenic variant C/T snv 7.0E-02 2
rs1461494 11 123055777 downstream gene variant T/A;C snv 2
rs1836778 4 29332870 intergenic variant T/C snv 0.56 2
rs1966678 4 29322410 intergenic variant T/G snv 0.60 2
rs2226150 6 77349634 intergenic variant G/A snv 0.49 2
rs4435343 18 43322011 intergenic variant C/A;T snv 2
rs4936767 11 123047451 upstream gene variant A/G snv 0.34 2
rs55920741 4 29331415 intergenic variant C/T snv 0.39 2
rs57580384 8 26048063 upstream gene variant G/A snv 0.14 2
rs59926619 8 26050704 intergenic variant G/A snv 0.13 2
rs638436 11 56495636 upstream gene variant G/A snv 0.58 2
rs638452 11 56495642 upstream gene variant A/T snv 0.58 2
rs6448638 4 29333941 intergenic variant T/C snv 0.56 2
rs72609945 8 26048781 upstream gene variant C/A;T snv 0.13 2
rs72749479 9 80667356 intergenic variant T/C snv 8.5E-02 2
rs72749483 9 80670259 intergenic variant T/C snv 8.5E-02 2
rs79666748 18 43280443 upstream gene variant A/C snv 7.0E-02 2
rs9341664 6 77375469 intergenic variant A/C snv 0.51 2
rs10041590
C5orf17
5 24064827 intron variant T/C;G snv 2
rs10054178
C5orf17
5 24059742 intron variant A/G snv 7.5E-02 2
rs10056373
C5orf17
5 24069684 intron variant C/T snv 7.4E-02 2
rs113051092
C5orf17
5 24060490 intron variant A/T snv 7.4E-02 2
rs16893073
C5orf17
5 24072508 intron variant C/G;T snv 2
rs73055009
C5orf17
5 24058406 intron variant A/G snv 7.5E-02 2