Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs917927904
PTEN ; KLLN
1.000 0.160 10 87864242 5 prime UTR variant G/T snv 7.0E-06 2
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs78245253
GATA2
1.000 3 128485850 missense variant G/A;C snv 4.0E-06; 5.0E-03 2
rs779530981
PTEN
1.000 0.160 10 87933035 missense variant C/A snv 4
rs777017502
CEBPZ
0.925 0.080 2 37222420 missense variant T/C;G snv 4.2E-06; 4.2E-06 3
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs770692189
BCL2L11 ; MIR4435-2HG
1.000 0.120 2 111123957 missense variant G/A;T snv 1.6E-05; 4.0E-06 2
rs767464424
CEBPZ
0.925 0.080 2 37222420 frameshift variant T/- delins 4.2E-06 3
rs7656411
TLR2
0.790 0.320 4 153706503 downstream gene variant T/G snv 0.35 8
rs757874631
CBL
0.882 0.120 11 119278211 missense variant T/A;C snv 4
rs757333753
RAF1
0.851 0.200 3 12618681 missense variant C/A;T snv 4.0E-06 6
rs724159947
ETV6
0.851 0.120 12 11869601 missense variant C/T snv 6
rs724159946
ETV6
1.000 12 11884541 missense variant G/A snv 7.0E-06 3
rs724159945
ETV6
1.000 12 11885968 missense variant C/A;T snv 3
rs61754966
NBN
0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 23
rs5743551
TLR1
0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs397507514
PTPN11
0.790 0.240 12 112450408 missense variant G/C;T snv 10
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs3921
CXCL10 ; ART3
0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs387906664
CBL
1.000 11 119278220 missense variant T/C;G snv 2
rs3745274
CYP2B6
0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30