Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1019221239
rs1019221239
APC
3 0.925 0.120 5 112835093 stop gained T/A;C;G snv 4.0E-06 0.700 1.000 1 1997 1997
dbSNP: rs1019340046
rs1019340046
TP53
5 0.882 0.080 17 7674225 missense variant C/T snv 0.700 1.000 4 1996 2009
dbSNP: rs1021662947
rs1021662947
PALB2
1 16 23614039 stop gained G/A snv 0.700 0
dbSNP: rs1023534466
rs1023534466
MSH6 ; FBXO11
1 2 47795984 frameshift variant TAAA/- delins 0.700 0
dbSNP: rs1025339570
rs1025339570
ATM
1 11 108249045 stop gained G/A;T snv 7.0E-06 0.700 0
dbSNP: rs1028347439
rs1028347439
BRIP1
1 17 61801267 stop gained G/A snv 0.700 0
dbSNP: rs104886456
rs104886456
FANCC
3 0.925 0.120 9 95172033 splice region variant T/A snv 2.9E-04 2.1E-04 0.700 1.000 10 1993 2016
dbSNP: rs104886457
rs104886457
FANCC ; AOPEP
4 0.882 0.240 9 95101742 stop gained G/A snv 5.2E-05 7.7E-05 0.700 1.000 5 1993 2017
dbSNP: rs104893825
rs104893825
VHL
2 1.000 0.120 3 10149819 missense variant G/T snv 0.700 1.000 8 1996 2010
dbSNP: rs104893826
rs104893826
VHL
4 0.882 0.200 3 10142038 missense variant G/A;C snv 0.700 1.000 7 1998 2014
dbSNP: rs104893830
rs104893830
VHL
3 0.925 0.160 3 10146561 missense variant G/C;T snv 0.700 1.000 5 1996 2014
dbSNP: rs104893831
rs104893831
VHL
4 0.925 0.040 3 10146549 missense variant G/A;C;T snv 2.0E-05 0.700 1.000 3 2011 2014
dbSNP: rs104894094
rs104894094
CDKN2A
12 0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06 0.700 0
dbSNP: rs104894095
rs104894095
CDKN2A
6 0.827 0.120 9 21971200 missense variant C/G;T snv 9.0E-06 0.700 1.000 16 1995 2010
dbSNP: rs104894097
rs104894097
CDKN2A
8 0.807 0.240 9 21974757 missense variant C/A;G;T snv 1.7E-05; 1.3E-05 0.700 1.000 19 1995 2015
dbSNP: rs104894098
rs104894098
CDKN2A
5 0.851 0.200 9 21970982 missense variant A/T snv 0.700 1.000 9 1994 2013
dbSNP: rs104894099
rs104894099
CDKN2A
5 0.851 0.200 9 21971183 missense variant A/C;T snv 4.6E-06 0.700 1.000 8 1998 2011
dbSNP: rs104894109
rs104894109
CDKN2A
3 0.925 0.120 9 21971192 missense variant C/A;T snv 0.700 1.000 9 1998 2011
dbSNP: rs104894259
rs104894259
MEN1 ; MAP4K2
2 1.000 0.120 11 64805078 missense variant A/G;T snv 0.700 0
dbSNP: rs104894261
rs104894261
MEN1 ; MAP4K2
2 1.000 0.120 11 64804588 stop gained G/A snv 0.700 1.000 2 1997 2012
dbSNP: rs104894263
rs104894263
MEN1
2 1.000 0.120 11 64809695 missense variant G/C snv 0.700 1.000 6 1997 2013
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
2 1.000 0.120 11 64805132 missense variant C/A;G;T snv 0.700 1.000 3 2004 2016
dbSNP: rs104894266
rs104894266
MEN1
2 1.000 0.120 11 64807557 stop gained G/A snv 0.700 1.000 2 1997 1997
dbSNP: rs104894267
rs104894267
MEN1 ; MAP4K2
2 1.000 0.120 11 64804789 stop gained G/A;T snv 7.0E-06 0.700 0
dbSNP: rs104894302
rs104894302
SDHD
5 0.851 0.200 11 112089002 missense variant A/G;T snv 4.0E-06 0.700 1.000 3 2000 2012