Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs1888747
FRMD3
1.000 0.120 9 83540636 upstream gene variant C/G snv 0.78 2
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs2607420
ITPKC
0.925 0.120 19 40738982 intron variant G/A snv 0.76 3
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs426496
LOC101927318 ; AQP2
1.000 0.040 12 49954295 synonymous variant T/C snv 0.77 0.71 3
rs2228226
GLI1 ; ARHGAP9
0.851 0.160 12 57472038 missense variant G/C snv 0.60 0.68 6
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 7
rs841853
SLC2A1
0.882 0.200 1 42935767 intron variant A/C snv 0.66 4
rs2856717 1.000 0.120 6 32702531 downstream gene variant A/G snv 0.64 2
rs2053044
ADRB2
1.000 0.040 5 148825809 5 prime UTR variant A/G snv 0.59 5
rs741301
ELMO1
0.925 0.160 7 36878390 intron variant C/T snv 0.59 3
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs237025
SUMO4 ; TAB2
0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs9896208
ACE
17 63498748 intron variant T/C snv 0.57 1
rs2412971
HORMAD2
0.882 0.320 22 30098382 intron variant G/A snv 0.55 5
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 5
rs3752462
MYH9
0.827 0.160 22 36314138 splice region variant T/C snv 0.57 0.53 7
rs136161
APOL1
0.925 0.160 22 36261386 intron variant G/C snv 0.51 3
rs653747
LINC00923
15 97659878 intron variant C/T snv 0.48 2
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs11089788
MYH9
0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs4293
ACE
17 63478305 non coding transcript exon variant G/A snv 0.45 1
rs739401
CARS1
11 3015094 intron variant C/T snv 0.45 2