Disease: Chronic kidney disease stage 5
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10137082
IL25
0.925 0.080 14 23370824 upstream gene variant C/T snv 0.23 2
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1033182
ESR1
0.882 0.160 6 151873899 intron variant G/A snv 0.26 3
rs10404257
ACTN4
0.925 0.080 19 38645846 upstream gene variant G/A snv 0.50 2
rs10808565
PVT1
0.925 0.080 8 127995166 non coding transcript exon variant C/T snv 0.31 2
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs10951982
RAC1
0.851 0.160 7 6382925 intron variant G/A;T snv 5
rs11089788
MYH9
0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs11571317
CTLA4
0.882 0.160 2 203867285 upstream gene variant C/T snv 5.2E-02 3
rs1162592300
ALB
0.925 0.080 4 73412045 missense variant G/A snv 3
rs12137135 0.925 0.080 1 22348728 intergenic variant A/C;G snv 2
rs12197043 0.882 0.160 6 149130141 regulatory region variant A/G snv 0.37 3
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs12431381
RTN1
0.925 0.080 14 59643053 intron variant T/C snv 0.35 2
rs12434215
RTN1
0.882 0.160 14 59642862 intron variant A/G snv 0.33 3
rs12437854
LOC107983974
0.925 0.080 15 93598604 intron variant T/G snv 0.10 2
rs12513649 0.851 0.160 5 173045049 regulatory region variant C/G;T snv 6
rs12917114 0.925 0.080 15 47852953 intron variant C/T snv 8.9E-02 2
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs13447075
PVT1
0.882 0.120 8 127998344 non coding transcript exon variant C/A snv 4
rs1452199941
TBC1D9
0.827 0.160 4 140670787 missense variant T/C snv 7.0E-06 5
rs1516792
IL1A
0.925 0.080 2 112778356 intron variant G/A snv 2
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38