Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1372399305
ACAN
1.000 0.160 15 88847281 missense variant T/A;C snv 1
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 20
rs397507483
BRAF
0.790 0.400 7 140753348 missense variant C/A;T snv 13
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 12
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv 10
rs387906660
BRAF
0.790 0.280 7 140801550 missense variant G/A;C;T snv 7
rs180177038
BRAF
0.851 0.200 7 140778007 missense variant C/G;T snv 4
rs180177034
BRAF
0.882 0.200 7 140801536 missense variant C/G snv 3
rs397507469
BRAF
0.882 0.200 7 140801503 missense variant G/T snv 3
rs180177036
BRAF
0.925 0.200 7 140778053 missense variant C/A;G snv 2
rs397507477
BRAF
1.000 0.160 7 140777995 missense variant G/A snv 2
rs397516903
BRAF
0.925 0.200 7 140801533 missense variant A/C;G snv 2
rs397516904
BRAF
0.925 0.200 7 140801487 missense variant T/C;G snv 2
rs727502904
BRAF
0.925 0.200 7 140734763 missense variant G/A;T snv 2
rs727504375
BRAF
0.925 0.200 7 140778059 missense variant T/G snv 2
rs397509343
BRAF
1.000 0.160 7 140801531 missense variant A/C snv 1
rs397516891
BRAF
1.000 0.160 7 140781599 missense variant G/C snv 1
rs397516905
BRAF
1.000 0.160 7 140801479 missense variant C/G snv 1
rs397517077
CBL
0.851 0.320 11 119278162 splice acceptor variant AAAG/- del 10
rs397517076
CBL
0.925 0.160 11 119278165 splice acceptor variant G/C;T snv 3
rs727504426
CBL
0.882 0.320 11 119278508 splice acceptor variant A/G snv 3
rs727504504
CBL
1.000 0.160 11 119278169 missense variant C/A snv 1
rs867983497
COMP
1.000 0.160 19 18785986 missense variant G/A;T snv 4.0E-06 1
rs746830376
EPHB2
0.925 0.200 1 22784501 missense variant G/A snv 2.4E-05 3.5E-05 4