Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs672601334
RIT1
0.752 0.400 1 155904798 missense variant G/C snv 18
rs730881014
RIT1
0.776 0.360 1 155904494 stop gained A/C;G;T snv 15
rs869025195
RIT1
0.790 0.280 1 155904493 missense variant T/G snv 11
rs869025191
RIT1
0.827 0.160 1 155904739 missense variant C/A;G;T snv 9
rs1557962794
RIT1
0.882 0.160 1 155910693 missense variant T/G snv 4
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
rs672601335
RIT1
0.882 0.160 1 155904456 missense variant C/G 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
rs397517148
SOS1
0.776 0.200 2 39023128 missense variant C/T snv 27
rs137852814
SOS1
0.752 0.240 2 39022774 missense variant T/A;C snv 4.0E-06 16
rs397517154
SOS1
0.763 0.280 2 39022773 missense variant C/A;G;T snv 4.0E-06 16
rs267607079
SOS1
0.776 0.240 2 39022772 missense variant C/A;G snv 13
rs137852813
SOS1
0.807 0.200 2 39051202 missense variant A/C;G snv 11
rs397517150
SOS1
0.827 0.160 2 39023118 missense variant A/C;G snv 7
rs727505381
SOS1
0.925 0.160 2 39013523 missense variant A/G snv 4.0E-06 5
rs137852812
SOS1
0.851 0.200 2 39051211 missense variant G/T snv 4
rs80338796
RAF1
0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 37
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