Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913450
ABL1
1.000 0.080 9 130873016 missense variant A/G snv 1
rs121913451
ABL1
0.851 0.160 9 130872903 missense variant C/A;G snv 4
rs121913452
ABL1
0.851 0.080 9 130873027 missense variant T/A;C;G snv 4
rs121913453
ABL1
1.000 0.080 9 130862962 missense variant G/A snv 1
rs121913454
ABL1
0.925 0.080 9 130874969 missense variant A/G snv 2
rs121913455
ABL1
1.000 0.080 9 130862955 missense variant C/G snv 1
rs121913456
ABL1
1.000 0.080 9 130862943 missense variant A/G snv 1
rs121913457
ABL1
1.000 0.080 9 130873004 missense variant T/C snv 1
rs121913458
ABL1
1.000 0.080 9 130862969 missense variant G/C;T snv 1
rs121913459
ABL1
0.672 0.160 9 130872896 missense variant C/T snv 25
rs121913460
ABL1
0.925 0.080 9 130862971 missense variant A/T snv 2
rs121913461
ABL1
0.851 0.120 9 130862970 missense variant T/C snv 5
rs121913505
KIT
0.925 0.080 4 54695598 missense variant G/A snv 2.0E-05 2
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49
rs121913516
KIT
1.000 0.080 4 54729353 missense variant C/T snv 4.0E-06 6
rs121913615
MPL
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06 25
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs12343867
INSL6 ; JAK2
0.790 0.200 9 5074189 intron variant T/C snv 0.25 9
rs1239681664
ABCA1
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs1250394819
LOC101927100 ; TMED7-TICAM2 ; TMED7
0.807 0.240 5 115616325 missense variant C/T snv 4.0E-06 9
rs1257378
LOC105369438 ; PIWIL4
1.000 0.080 11 94621792 intron variant A/T snv 1
rs12573787
KLLN ; PTEN
1.000 0.080 10 87863959 5 prime UTR variant G/A;C snv 1
rs1314838108
ABL1
0.925 0.160 9 130854977 missense variant G/A snv 7.0E-06 2
rs1343187782
GOLGA4
1.000 0.080 3 37298923 missense variant T/C snv 4.0E-06 1
rs1353702185
MDM2
0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79