Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2289030
MIR492 ; KRT19P2
0.882 0.120 12 94834510 non coding transcript exon variant G/C snv 9.7E-02 6.3E-02 6
rs16851720
RNF7
0.827 0.120 3 141744456 intron variant A/C snv 0.21 5
rs2645424
FDFT1
0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs843645
ACYP2
0.827 0.120 2 54247527 intron variant T/A;G snv 0.19 5
rs121918664
TERT
0.851 0.120 5 1254395 missense variant C/T snv 5.2E-05 9.1E-05 4
rs10945859
PRKN
0.882 0.120 6 162721570 intron variant T/C snv 0.17 3
rs1431315635
HFE ; LOC108783645
0.882 0.120 6 26092928 missense variant C/T snv 4.0E-06 3
rs1485766
VEGFC ; LOC105377555
0.882 0.120 4 176689730 intron variant T/A;G snv 3
rs376373278
MPO
0.882 0.120 17 58279015 missense variant G/A;C snv 4.2E-06 3
rs3820998
TANK ; LOC105373719
0.882 0.120 2 161138615 intron variant C/A;T snv 3
rs3844942 0.882 0.120 4 189571800 intergenic variant T/C snv 3
rs3859501
MIR371B ; MIR373 ; MIR372 ; MIR371A
0.882 0.120 19 53788157 non coding transcript exon variant A/C snv 0.43 3
rs755284374
HFE
0.882 0.120 6 26093122 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs767864210
PDLIM5
0.882 0.120 4 94657500 missense variant G/A;T snv 8.0E-05 2.1E-05 3
rs897206619
HFE
0.882 0.120 6 26093128 missense variant C/T snv 3.5E-05 3
rs972427414
MPO
0.882 0.120 17 58279379 missense variant A/G snv 3
rs1469557
LOC101929248
0.925 0.120 8 10849291 downstream gene variant C/T snv 0.18 2
rs1545224
FABP1
0.925 0.120 2 88124297 3 prime UTR variant A/G snv 0.18 2
rs2629751
GLT8D2
0.925 0.120 12 104028030 intron variant A/G snv 0.36 2
rs642588
IGF2R
0.925 0.120 6 159990235 intron variant A/G snv 0.83 2
rs747432300
GPT ; LOC101928953
0.925 0.120 8 144504357 missense variant C/A;T snv 8.1E-06; 1.2E-04 2
rs9380516 0.925 0.120 6 35534425 TF binding site variant T/C snv 0.85 2
rs17580
SERPINA1
0.776 0.160 14 94380925 missense variant T/A snv 2.3E-02 2.9E-02 14
rs236918
PCSK7
0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 10