Disease: Creatinine measurement, serum (procedure)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143193096
IGF1R
15 98916098 missense variant G/A;C snv 8.4E-05; 4.0E-06 3
rs151134704
NFKB1 ; LOC105377347
4 102616435 splice region variant C/T snv 1.6E-04 9.1E-05 3
rs16856823
LRP2
2 169343942 intron variant A/T snv 4.6E-02 3
rs199592697
WNT7A
3 13854632 missense variant C/T snv 1.7E-04 1.1E-04 3
rs2453580
SLC47A1
17 19535008 non coding transcript exon variant T/C snv 0.37 4
rs6026578
GNAS ; LOC101927932
20 58888417 5 prime UTR variant C/G snv 0.60 4
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs1106766
R3HDM2
0.882 0.120 12 57415673 intron variant C/T snv 0.19 7
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 7
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 9
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 7
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 10
rs10851885
NRG4
0.925 0.120 15 76012162 5 prime UTR variant A/G snv 0.18 5
rs10994856
A1CF
0.925 0.120 10 50885488 intron variant G/A snv 0.19 5
rs10994860
A1CF
0.925 0.120 10 50885664 5 prime UTR variant C/T snv 0.19 5
rs149454410
SLC2A9
0.925 0.120 4 9942000 missense variant C/G;T snv 4.0E-05; 3.2E-04 5
rs186459505
SFMBT1
0.925 0.120 3 52907083 missense variant G/A;T snv 1.1E-04; 4.0E-06 5
rs3741414
INHBC
0.925 0.120 12 57450266 3 prime UTR variant C/T snv 0.19 7
rs729761
LOC105375069 ; LOC107986598
0.925 0.120 6 43836834 intron variant T/A;G snv 6
rs963837
LOC101928338 ; LINC02859
0.925 0.120 11 30727543 intergenic variant T/C snv 0.35 8
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 5
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9