Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 1
rs1057519825
BTK
0.882 0.120 X 101356176 missense variant C/G snv 1
rs1057519826
BTK
0.882 0.120 X 101356177 missense variant A/T snv 1
rs1057519831
PLCG2
1.000 0.120 16 81912655 missense variant C/T snv 1
rs1057519832
PLCG2
1.000 0.120 16 81928578 missense variant A/C;G;T snv 1
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 1
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs1057519896
FBXW7
0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs1057519959
SF3B2
0.882 0.200 11 66063028 missense variant A/C snv 4
rs1057519960
SF3B2
0.827 0.280 11 66063413 missense variant A/G snv 7
rs1057519961
SF3B1
0.851 0.240 2 197402759 missense variant C/T snv 4
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 13
rs1057519995
TP53
0.807 0.240 17 7674200 missense variant T/A snv 8
rs1057519997
TP53
0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs1057520009
XPO1
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 5
rs1057520010
XPO1
0.882 0.200 2 61492336 missense variant T/A;G snv 5
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 1
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 25