Disease: Creatinine measurement, serum (procedure)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 10
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 9
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs2337106
SMAD7
18 48934533 intron variant C/A;G snv 4
rs863678
HOXD10 ; HOXD11
2 176109376 3 prime UTR variant G/T snv 0.69 3