Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1057519771
ABL1
1.000 0.080 9 130872201 missense variant G/C snv 2
rs111340708
ATXN2 ; SH2B3
0.925 0.080 12 111447548 intron variant TGGGGTGGGGTGGGG/-;TGGGG;TGGGGTGGGG;TGGGGTGGGGTGGGGTGGGG;TGGGGTGGGGTGGGGTGGGGTGGGG delins 0.52 2
rs121913454
ABL1
0.925 0.080 9 130874969 missense variant A/G snv 2
rs121913460
ABL1
0.925 0.080 9 130862971 missense variant A/T snv 2
rs1314838108
ABL1
0.925 0.160 9 130854977 missense variant G/A snv 7.0E-06 2
rs1483790387
TMED7-TICAM2 ; TMED7
0.925 0.120 5 115625762 missense variant C/A snv 2
rs918140013
ATXN2 ; SH2B3
0.925 0.080 12 111447663 missense variant G/A snv 7.0E-06 2
rs1057519758
ABL1
1.000 0.080 9 130872153 missense variant T/G snv 1
rs1057519772
ABL1
1.000 0.080 9 130872895 missense variant A/G snv 1
rs1057519774
ABL1
1.000 0.080 9 130872902 missense variant T/G snv 1
rs1057519775
ABL1
1.000 0.080 9 130873028 missense variant T/G snv 1
rs1057519776
CSF3R
1.000 0.080 1 36467843 missense variant T/C snv 1
rs1178702025
SETBP1
1.000 0.080 18 44951912 missense variant G/A snv 1
rs121913449
ABL1
1.000 0.080 9 130862977 missense variant A/T snv 1
rs121913450
ABL1
1.000 0.080 9 130873016 missense variant A/G snv 1
rs121913453
ABL1
1.000 0.080 9 130862962 missense variant G/A snv 1
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
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
rs1487152821
COL11A2
1.000 0.080 6 33180274 missense variant G/A snv 7.0E-06 1