Disease: Multiple Myeloma
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894340
CDK4
0.827 0.200 12 57751647 missense variant C/A;T snv 5
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs770248150
KRAS
0.807 0.240 12 25225713 missense variant T/A;G snv 4.0E-06 6
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
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
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 13
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 11
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs11547328
CDK4
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 6
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 9
rs180177040
BRAF
0.790 0.360 7 140754187 missense variant T/C;G snv 9
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
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
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 6
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 15
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 14
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 12
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 19
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
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
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 17