Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 28
rs104893626
CXCR4 ; LOC112268426
0.827 0.280 2 136114915 stop gained G/C snv 11
rs773862672
MTOR
0.882 0.280 1 11247922 missense variant G/A;C snv 1.2E-05 6
rs1392080411
KLF2
0.827 0.160 19 16325934 missense variant C/T snv 7.0E-06 5
rs757085537
PRDM1 ; ATG5
0.851 0.160 6 106105356 missense variant C/T snv 7.0E-06 5
rs116446171 0.851 0.160 6 484453 downstream gene variant C/G snv 2.3E-02 4
rs1242982981
CLEC12A
0.851 0.160 12 9984989 missense variant C/T snv 4
rs1472503583
PWWP3A
0.925 0.160 19 1360712 missense variant C/T snv 4.0E-06 4
rs117410836 0.925 0.160 14 95585637 downstream gene variant T/C snv 2.4E-02 2
rs574384780
BCR ; RSPH14
1.000 0.160 22 23181886 missense variant T/A;C snv 2.7E-04; 4.0E-06 1
rs179159
SYNE3
1.000 0.160 14 95506111 intergenic variant A/G;T snv 1