Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80338796
RAF1
0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 37
rs180177035
BRAF
0.752 0.280 7 140801502 missense variant T/C snv 35
rs397517148
SOS1
0.776 0.200 2 39023128 missense variant C/T snv 27
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 20
rs397507547
PTPN11
0.752 0.280 12 112489086 missense variant A/G snv 4.0E-06 14
rs397507483
BRAF
0.790 0.400 7 140753348 missense variant C/A;T snv 13
rs397507478
BRAF
0.790 0.440 7 140777014 missense variant C/A snv 12