Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2053044
ADRB2
1.000 0.040 5 148825809 5 prime UTR variant A/G snv 0.59 5
rs267606743
COL4A1
1.000 0.160 13 110192222 missense variant C/T snv 5
rs426496
LOC101927318 ; AQP2
1.000 0.040 12 49954295 synonymous variant T/C snv 0.77 0.71 3
rs9974610 1.000 0.080 21 31646056 intergenic variant A/G snv 0.13 3
rs11122576
AGT
1.000 0.080 1 230710933 intron variant T/C snv 8.2E-02 2
rs121912863
COL4A4
1.000 2 227008112 missense variant G/A snv 1.6E-04 1.8E-04 2
rs146956976
GSN
1.000 0.080 9 121302985 missense variant C/T snv 3.1E-04 4.0E-04 2
rs1888747
FRMD3
1.000 0.120 9 83540636 upstream gene variant C/G snv 0.78 2
rs1926723
AGT
1.000 0.080 1 230704350 intron variant T/A;C;G snv 1.2E-05; 0.11; 2.0E-05 2
rs2856717 1.000 0.120 6 32702531 downstream gene variant A/G snv 0.64 2
rs3115573 1.000 0.120 6 32251066 upstream gene variant A/G snv 0.41 2
rs3729548
SLC2A1
1.000 0.080 1 42934681 intron variant C/T snv 0.32 2
rs6610650 1.000 0.040 X 37777261 intron variant G/A snv 0.27 2
rs7704116
PPP2CA
1.000 0.080 5 134216763 intron variant C/T snv 9.9E-02 2
rs868580411
COL4A5
1.000 X 108602973 missense variant G/A;T snv 2
rs9357155
PSMB8
1.000 0.120 6 32842071 non coding transcript exon variant G/A;C snv 2
rs758564400
REN
0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06 5
rs2248098
VDR
0.925 0.120 12 47859573 intron variant A/G;T snv 4
rs1191455921
LMX1B
0.925 0.240 9 126693319 missense variant G/A snv 3
rs121918673
HNF1B
0.925 0.200 17 37701122 missense variant G/C snv 1.9E-05 3
rs12449782 0.925 0.200 17 63498888 intron variant G/A snv 0.41 3
rs136161
APOL1
0.925 0.160 22 36261386 intron variant G/C snv 0.51 3
rs1883414
HLA-DPB2
0.925 0.200 6 33118671 non coding transcript exon variant G/A snv 0.28 3
rs2281999
UNC13B
0.925 0.160 9 35381507 intron variant C/T snv 0.35 0.38 3
rs2607420
ITPKC
0.925 0.120 19 40738982 intron variant G/A snv 0.76 3