Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs587778720
rs587778720
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1992 1992
dbSNP: rs121908859
rs121908859
1.000 0.040 14 81143914 missense variant A/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1993 1993
dbSNP: rs1057520001
rs1057520001
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1995 1995
dbSNP: rs139085046
rs139085046
7 141972869 missense variant C/T snv 1.6E-04 1.7E-04
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1995 1995
dbSNP: rs147506929
rs147506929
NF2
22 29678208 missense variant A/C;G snv 8.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1995 1995
dbSNP: rs200246711
rs200246711
2 219216057 missense variant C/A;T snv 2.0E-04
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1995 1995
dbSNP: rs536976542
rs536976542
20 58854270 missense variant G/A;T snv 8.2E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1995 1995
dbSNP: rs76262710
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1995 1995
dbSNP: rs770251749
rs770251749
1.000 0.120 6 54121506 missense variant A/C snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1995 1995
dbSNP: rs79781594
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1995 1995
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1995 1995
dbSNP: rs2227564
rs2227564
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1997 1997
dbSNP: rs121913243
rs121913243
MET
0.827 0.160 7 116777410 missense variant A/C;G snv 1.2E-05
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1998 1998
dbSNP: rs121913403
rs121913403
0.683 0.240 3 41224622 missense variant C/A;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1998 1998
dbSNP: rs137853296
rs137853296
RB1
1.000 0.080 13 48463758 missense variant T/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1998 1998
dbSNP: rs17653265
rs17653265
1.000 0.040 6 121447605 missense variant C/T snv 8.1E-03 9.1E-03
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1998 1998
dbSNP: rs749280481
rs749280481
0.925 0.160 11 2922102 missense variant G/A snv 1.3E-04 1.4E-04
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1998 1998
dbSNP: rs1057519710
rs1057519710
KIT
0.695 0.280 4 54733166 missense variant G/C;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1999 1999
dbSNP: rs1114167494
rs1114167494
1.000 0.120 11 64808031 missense variant C/A snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1999 1999
dbSNP: rs121913413
rs121913413
0.763 0.240 3 41224634 missense variant C/A;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1999 1999
dbSNP: rs121913506
rs121913506
KIT
0.677 0.320 4 54733154 missense variant G/A;C;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1999 1999
dbSNP: rs137853080
rs137853080
1.000 0.040 19 1207058 missense variant T/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1999 1999
dbSNP: rs139142865
rs139142865
1.000 0.120 12 51920826 missense variant C/T snv 1.6E-03 2.0E-03
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1999 1999
dbSNP: rs1474630243
rs1474630243
1 155209072 missense variant G/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1999 1999
dbSNP: rs34012126
rs34012126
7 100855831 frameshift variant G/- delins
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1999 1999