Disease: Multiple Myeloma
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 23
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs104894340
CDK4
0.827 0.200 12 57751647 missense variant C/A;T snv 5
rs1057519877
B2M ; PATL2
0.763 0.280 15 44711549 start lost G/A snv 10
rs1057519879
PATL2 ; B2M
0.763 0.280 15 44711548 start lost T/C;G snv 10
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 13
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 12
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 12
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 11
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 6
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 9
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 16
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs180177040
BRAF
0.790 0.360 7 140754187 missense variant T/C;G snv 9
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 17
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 20