Disease: Multiple Myeloma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs267606870
IDH2
0.763 0.280 15 90088703 missense variant G/A;C snv 11
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 16
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 22
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 25
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 16
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 19