Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 12
rs180177042
BRAF
0.807 0.280 7 140749365 missense variant A/C;T snv 8
rs387906660
BRAF
0.790 0.280 7 140801550 missense variant G/A;C;T snv 7
rs387906661
BRAF
0.807 0.280 7 140801551 missense variant T/G snv 6
rs397507466
BRAF
0.807 0.280 7 140801537 missense variant T/A;C;G snv 4.0E-06 6
rs397516895
BRAF
0.827 0.280 7 140753392 missense variant A/T snv 5
rs180177034
BRAF
0.882 0.200 7 140801536 missense variant C/G snv 3
rs606231228
BRAF
0.925 0.160 7 140777013 missense variant C/A;G snv 2
rs267606706
CBL
0.807 0.240 11 119278181 missense variant T/A;C snv 8.0E-06 9
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs121908595
MAP2K1
0.827 0.280 15 66436843 missense variant A/G snv 4.0E-06 8
rs876657651
MAP2K1
0.882 0.160 15 66436818 missense variant A/G snv 3
rs267606920
NRAS
0.882 0.160 1 114713911 missense variant C/T snv 7.0E-06 4
rs267606921
NRAS
0.882 0.160 1 114713941 missense variant G/A snv 3
rs397514553
NRAS
0.925 0.200 1 114716060 missense variant G/A snv 2
rs869025573
NRAS
1.000 0.160 1 114716090 missense variant A/T snv 2
rs564251686
PLAAT4
1.000 0.160 11 63544632 missense variant G/A snv 4.4E-05 6.3E-05 1
rs121918459
PTPN11
0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 47
rs397507520
PTPN11
0.658 0.520 12 112453279 missense variant G/C;T snv 39
rs121918455
PTPN11
0.695 0.440 12 112477720 missense variant A/C;G snv 31
rs121918460
PTPN11
0.708 0.400 12 112450364 missense variant T/A;G snv 4.0E-06 27
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs121918457
PTPN11
0.701 0.280 12 112488466 missense variant C/T snv 4.0E-06 7.0E-06 24
rs121918467
PTPN11
0.807 0.280 12 112486482 missense variant C/A;T snv 8.0E-06; 1.2E-05 23
rs397507545
PTPN11
0.708 0.560 12 112489083 missense variant G/A;C snv 4.0E-06 20