Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs868580411
COL4A5
1.000 X 108602973 missense variant G/A;T snv 2
rs1888747
FRMD3
1.000 0.120 9 83540636 upstream gene variant C/G snv 0.78 2
rs146956976
GSN
1.000 0.080 9 121302985 missense variant C/T snv 3.1E-04 4.0E-04 2
rs653747
LINC00923
15 97659878 intron variant C/T snv 0.48 2
rs7704116
PPP2CA
1.000 0.080 5 134216763 intron variant C/T snv 9.9E-02 2
rs9357155
PSMB8
1.000 0.120 6 32842071 non coding transcript exon variant G/A;C snv 2
rs3729548
SLC2A1
1.000 0.080 1 42934681 intron variant C/T snv 0.32 2
rs12449782 0.925 0.200 17 63498888 intron variant G/A snv 0.41 3
rs9974610 1.000 0.080 21 31646056 intergenic variant A/G snv 0.13 3
rs4309
ACE
0.925 0.120 17 63482562 synonymous variant C/T snv 0.46 0.36 3
rs136161
APOL1
0.925 0.160 22 36261386 intron variant G/C snv 0.51 3
rs741301
ELMO1
0.925 0.160 7 36878390 intron variant C/T snv 0.59 3
rs1883414
HLA-DPB2
0.925 0.200 6 33118671 non coding transcript exon variant G/A snv 0.28 3
rs121918673
HNF1B
0.925 0.200 17 37701122 missense variant G/C snv 1.9E-05 3
rs2607420
ITPKC
0.925 0.120 19 40738982 intron variant G/A snv 0.76 3
rs1191455921
LMX1B
0.925 0.240 9 126693319 missense variant G/A snv 3
rs426496
LOC101927318 ; AQP2
1.000 0.040 12 49954295 synonymous variant T/C snv 0.77 0.71 3
rs4972593
LOC107985961
0.925 0.200 2 173598126 intergenic variant T/A snv 0.20 3
rs55703767
MFF-DT ; COL4A3
0.925 0.160 2 227256385 missense variant G/A;T snv 4.0E-06; 0.17 3
rs28362930
SEMA7A
0.925 0.160 15 74408859 downstream gene variant G/A snv 0.16 3
rs3923647
TLR1
0.925 0.080 4 38797918 missense variant T/A;C;G snv 2.7E-02; 4.0E-06; 1.6E-05 3
rs2281999
UNC13B
0.925 0.160 9 35381507 intron variant C/T snv 0.35 0.38 3
rs841853
SLC2A1
0.882 0.200 1 42935767 intron variant A/C snv 0.66 4
rs2248098
VDR
0.925 0.120 12 47859573 intron variant A/G;T snv 4
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 5