Disease: Blood urea nitrogen measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 9
rs760077
MTX1 ; THBS3
0.925 0.120 1 155208991 missense variant T/A snv 0.36 8
rs963837
LOC101928338 ; LINC02859
0.925 0.120 11 30727543 intergenic variant T/C snv 0.35 8
rs3925584
LOC101928338
1.000 0.080 11 30738788 intergenic variant T/C snv 0.35 7
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs4886755
NRG4
0.925 0.120 15 76005791 non coding transcript exon variant A/G;T snv 0.49 6
rs12908437
IGF1R
0.882 0.200 15 98744146 intron variant T/C;G snv 5
rs6026578
GNAS ; LOC101927932
20 58888417 5 prime UTR variant C/G snv 0.60 4
rs73728279
PRKAG2
1.000 0.080 7 151714408 intron variant G/A;T snv 4
rs11940694
KLB
4 39413373 intron variant A/G snv 0.57 3
rs13230625 1.000 0.080 7 1246608 regulatory region variant G/A snv 0.62 3
rs12134456
GON4L
1 155752715 intron variant C/G snv 0.26 2
rs836968
FAIM2
12 49873552 intron variant C/T snv 0.31 2