Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs796065343
CSF3R
0.776 0.080 1 36467833 missense variant G/A snv 12
rs1057519753
JAK1
0.763 0.120 1 64846664 missense variant C/A snv 9
rs869312953
JAK1
0.851 0.120 1 64846735 missense variant G/T snv 5
rs1360698171
RNASEL
0.851 0.080 1 182584103 missense variant T/C snv 4
rs753000469
FLVCR1-DT ; FLVCR1
0.851 0.200 1 212859113 missense variant C/T snv 4.0E-06 4
rs2308950
CASP9
0.882 0.040 1 15507011 missense variant C/G;T snv 4.0E-06; 1.1E-02 3
rs201045130
NT5C1A
0.925 0.040 1 39659467 missense variant A/G snv 9.9E-05 1.0E-04 2
rs17433222
C1QB
1.000 0.040 1 22652153 upstream gene variant G/A snv 0.23 1
rs2228014
CXCR4
0.752 0.240 2 136115514 synonymous variant G/A snv 4.6E-02 3.5E-02 14
rs3116496
CD28
0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 11
rs10931910
AOX1
0.925 0.040 2 200659013 intron variant A/G;T snv 2
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49
rs3822214
KIT
0.732 0.240 4 54727298 missense variant A/C;G;T snv 7.7E-02; 8.0E-06 13
rs121913514
KIT
0.763 0.240 4 54733174 missense variant T/A;G snv 12
rs121913521
KIT
0.790 0.120 4 54727447 missense variant T/A;C;G snv 12
rs748843032
MTTP
0.807 0.160 4 99594840 missense variant T/C snv 4.0E-06 8
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48