Disease: Kidney Failure, Chronic
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
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 10
rs1171614
SLC16A9
0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79 7
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 7
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 7
rs881858
LOC105375069 ; LOC107986598
0.882 0.200 6 43838872 intron variant G/A;C snv 7
rs1171616
SLC16A9
0.882 0.200 10 59708831 intron variant G/T snv 0.79 6
rs4148155
ABCG2
0.882 0.200 4 88133515 intron variant A/G snv 8.7E-02 5
rs13111638
SLC2A9 ; LOC105374476
0.882 0.200 4 9995266 intron variant T/C snv 0.82 4
rs59834205
SLC2A9
0.882 0.200 4 9959396 intron variant -/GA delins 1.1E-04 3