Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10808565
PVT1
0.925 0.080 8 127995166 non coding transcript exon variant C/T snv 0.31 2
rs2236242
SERPINA12
0.776 0.280 14 94493715 intron variant T/A snv 0.31 9
rs2576178
RNLS ; LIPJ
0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 9
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs9349417
CD2AP
0.925 0.080 6 47612921 intron variant A/G snv 0.27 2
rs1033182
ESR1
0.882 0.160 6 151873899 intron variant G/A snv 0.26 3
rs1670754 0.882 0.160 4 32263375 intergenic variant G/A snv 0.24 3
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs3760106
PRKCB
0.925 0.080 16 23834475 upstream gene variant C/T snv 0.23 3
rs10137082
IL25
0.925 0.080 14 23370824 upstream gene variant C/T snv 0.23 2
rs3759126
AQP2
0.882 0.080 12 49950079 upstream gene variant A/G snv 0.23 3
rs9369717
CD2AP
0.925 0.080 6 47586732 intron variant T/G snv 0.22 2
rs3732379
CX3CR1
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs4730751
CAV1
0.882 0.120 7 116540796 intron variant C/A snv 0.22 4
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs9374
RAC1
0.925 0.080 7 6402740 3 prime UTR variant G/A snv 0.18 2
rs730497
GCK ; LOC105375257
0.882 0.160 7 44184122 intron variant G/A snv 0.17 4
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs16840252
CTLA4
0.776 0.480 2 203866796 upstream gene variant C/T snv 0.16 8
rs7918972
CUBN
0.925 0.080 10 16828293 intron variant T/G snv 0.15 2
rs1800454
TAP2
0.851 0.280 6 32832635 missense variant C/T snv 0.14 0.14 4
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11