Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs770692189
BCL2L11 ; MIR4435-2HG
1.000 0.120 2 111123957 missense variant G/A;T snv 1.6E-05; 4.0E-06 2
rs121918453
PTPN11
0.732 0.280 12 112450394 missense variant G/A;C;T snv 19
rs121918454
PTPN11
0.742 0.280 12 112450395 missense variant C/A;G;T snv 17
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs397507514
PTPN11
0.790 0.240 12 112450408 missense variant G/C;T snv 10
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 26
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs267606706
CBL
0.807 0.240 11 119278181 missense variant T/A;C snv 8.0E-06 9
rs757874631
CBL
0.882 0.120 11 119278211 missense variant T/A;C snv 4
rs387906664
CBL
1.000 11 119278220 missense variant T/C;G snv 2
rs757333753
RAF1
0.851 0.200 3 12618681 missense variant C/A;T snv 4.0E-06 6
rs78245253
GATA2
1.000 3 128485850 missense variant G/A;C snv 4.0E-06; 5.0E-03 2
rs2285489
ADAMTS13
9 133424254 intron variant T/C snv 0.68 2
rs1801271
CSF1R
5 150054082 missense variant T/A;C snv 2
rs121913393
CSF1R
5 150054083 missense variant A/G snv 2
rs1057519802
CSF1R
5 150061765 missense variant A/C snv 2
rs1057520014
CSF1R
5 150073480 missense variant C/A snv 1
rs121913390
CSF1R
5 150073481 stop gained A/G;T snv 2
rs7656411
TLR2
0.790 0.320 4 153706503 downstream gene variant T/G snv 0.35 8
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19