Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368927897
JAK2 ; INSL6
0.790 0.240 9 5072541 missense variant G/A;T snv 2.8E-05; 6.4E-05 9
rs10053538
HAVCR2
0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs57749775
KRT8
0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 6
rs1054690270
LOC101928953 ; GPT
0.827 0.160 8 144505907 frameshift variant CT/- delins 5
rs10932029
ICOS ; LOC101927840
0.827 0.200 2 203937045 intron variant T/A;C snv 5
rs1396171148
FARSB
0.851 0.200 2 222613892 missense variant T/G snv 5
rs1553554543
FARSB
0.851 0.200 2 222631606 missense variant T/C snv 5
rs3129859 0.827 0.320 6 32433162 intergenic variant G/C;T snv 5
rs5743314
TLR3
0.851 0.160 4 186079221 intron variant G/C;T snv 5
rs10433937
HSD17B13
0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs1346044973
TERT
0.851 0.160 5 1294158 missense variant G/A snv 1.1E-05 4
rs4656942
CD244
0.851 0.160 1 160861258 intron variant G/A;C;T snv 4
rs6715787
EPAS1
0.851 0.200 2 46349033 intron variant C/G;T snv 4
rs137853590
PHKG2
0.882 0.160 16 30751140 stop gained C/T snv 4.0E-06 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
rs26907
RASGRF2
0.882 0.240 5 81069496 intron variant G/A;T 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
rs755284374
HFE
0.882 0.120 6 26093122 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs972427414
MPO
0.882 0.120 17 58279379 missense variant A/G snv 3
rs1201810520
EIF2AK3
0.925 0.160 2 88590497 missense variant C/T snv 2
rs1227756
COL13A1
0.925 0.080 10 69828748 intron variant G/A;C snv 2
rs2298839
AFP
0.925 0.080 4 73445127 splice region variant A/G;T snv 0.54 2