Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs727503094
LRRC56 ; HRAS
0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs104894231
LRRC56 ; HRAS
0.776 0.360 11 533467 missense variant C/G;T snv 9
rs121917759
HRAS ; LRRC56
0.790 0.480 11 533466 missense variant G/A snv 8
rs121917757
HRAS ; LRRC56
0.851 0.200 11 534259 stop gained G/A;T snv 1.2E-05 4
rs121917758
LRRC56 ; HRAS
0.851 0.160 11 533883 missense variant G/A snv 4
rs730880460
LRRC56 ; HRAS
0.882 0.120 11 533877 missense variant C/A;T snv 3
rs121917756
LRRC56 ; HRAS
0.925 0.120 11 533869 missense variant C/T snv 2
rs727503093
LRRC56 ; HRAS
0.925 0.160 11 533881 missense variant C/T snv 2
rs104894227
HRAS ; LRRC56
1.000 0.080 11 533553 missense variant T/C snv 1
rs398122808
HRAS ; LRRC56
1.000 0.080 11 534210 coding sequence variant -/CTC delins 1
rs398122809
HRAS ; LRRC56
1.000 0.080 11 534212 inframe insertion -/TCT delins 1
rs35613389
LRRC56 ; HRAS
1.000 0.080 11 533309 frameshift variant G/-;GG delins 1
rs587777239
LRRC56 ; HRAS
1.000 0.080 11 533848 inframe insertion -/GTCCCGCATGGCGCTGTACTC delins 1
rs727504747
LRRC56 ; HRAS
1.000 0.080 11 533880 missense variant GC/AG mnv 1