Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507517
PTPN11
0.827 0.160 12 112450497 missense variant A/C snv 8
rs121918455
PTPN11
0.695 0.440 12 112477720 missense variant A/C;G snv 31
rs121918456
PTPN11
0.752 0.280 12 112473023 missense variant A/C;G snv 13
rs137852813
SOS1
0.807 0.200 2 39051202 missense variant A/C;G snv 11
rs121918470
PTPN11
0.790 0.160 12 112489105 missense variant A/C;G snv 4.0E-06 10
rs397517150
SOS1
0.827 0.160 2 39023118 missense variant A/C;G snv 7
rs730881014
RIT1
0.776 0.360 1 155904494 stop gained A/C;G;T snv 15
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 12
rs397507505
PTPN11
0.827 0.240 12 112450352 missense variant A/C;G;T snv 5
rs180177042
BRAF
0.807 0.280 7 140749365 missense variant A/C;T snv 8
rs121918459
PTPN11
0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 47
rs28933386
PTPN11
0.752 0.400 12 112477719 missense variant A/G snv 1.2E-05 7.0E-06 15
rs121918466
PTPN11
0.752 0.280 12 112450416 missense variant A/G snv 14
rs397507547
PTPN11
0.752 0.280 12 112489086 missense variant A/G snv 4.0E-06 14
rs121908595
MAP2K1
0.827 0.280 15 66436843 missense variant A/G snv 4.0E-06 8
rs397507501
PTPN11
0.882 0.160 12 112446385 missense variant A/G snv 5
rs397507529
PTPN11
0.851 0.160 12 112473031 missense variant A/G snv 7.0E-06 5
rs727505381
SOS1
0.925 0.160 2 39013523 missense variant A/G snv 4.0E-06 5
rs397507523
PTPN11
0.882 0.160 12 112472954 missense variant A/G snv 3
rs876657651
MAP2K1
0.882 0.160 15 66436818 missense variant A/G snv 3
rs397507504
PTPN11
0.925 0.160 12 112450346 missense variant A/G snv 7.0E-06 2
rs397516801
PTPN11
0.925 0.160 12 112450389 missense variant A/G snv 2
rs201787206
PTPN11
1.000 0.160 12 112477722 missense variant A/G snv 5.0E-04 2.5E-04 1
rs886043790
PTPN11
1.000 0.160 12 112450355 missense variant A/G snv 4.0E-06 7.0E-06 1
rs397516895
BRAF
0.827 0.280 7 140753392 missense variant A/T snv 5