Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs41293459
BRCA1
0.763 0.280 17 43063930 missense variant C/A;G;T snv 2.4E-05 12
rs55770810
BRCA1
0.763 0.280 17 43063931 missense variant G/A;T snv 2.4E-05; 8.0E-06 10
rs147105770
ERCC4
0.776 0.280 16 13935697 missense variant C/G;T snv 1.2E-05; 6.4E-05 8
rs80359065
BRCA2
0.827 0.240 13 32363389 missense variant G/A;T snv 7.9E-04 5
rs80359130
BRCA2
0.827 0.200 13 32376769 missense variant C/A;G;T snv 8.0E-06 5
rs765576835
FANCD2
0.882 0.200 3 10036306 missense variant T/C snv 4.0E-06 4
rs80359183
BRCA2
0.882 0.120 13 32380096 stop gained T/A;C snv 4
rs878853666
FANCA
0.882 0.200 16 89803299 missense variant G/A snv 4
rs121434426
FANCG
0.882 0.120 9 35076442 stop gained G/A snv 4.0E-06 3
rs1555524842
RFWD3
0.882 0.120 16 74628505 missense variant A/T snv 3
rs797045175
BRCA1
0.882 0.120 17 43095919 splice acceptor variant ACAC/- delins 3
rs1055368753
BRCA1
0.925 0.120 17 43092010 missense variant G/A snv 2
rs1057516430
FANCA
0.925 0.120 16 89811060 stop gained G/A snv 2
rs1060501887
FANCA ; ZNF276
0.925 0.120 16 89738881 splice donor variant C/T snv 2
rs1232171121
FANCA
0.925 0.120 16 89814519 splice donor variant C/A;T snv 2
rs1291524243
FANCA
0.925 0.120 16 89799203 stop gained G/A;C snv 4.0E-06 2
rs139235751
FANCA
0.925 0.120 16 89775768 missense variant C/G;T snv 2.4E-03; 2.0E-05 2
rs1432988639
ZNF276 ; FANCA
0.925 0.120 16 89740803 splice donor variant C/A;G;T snv 1.2E-05 2
rs1555540076
FANCA
0.925 0.120 16 89752223 splice acceptor variant C/G snv 2
rs1555548512
FANCA
0.925 0.120 16 89771722 stop gained G/A snv 2
rs1564719070
FANCC
0.925 0.120 9 95171081 frameshift variant C/- delins 2
rs367924414
AOPEP ; FANCC
0.925 0.120 9 95117321 missense variant G/A snv 2
rs574034197
FANCA
0.925 0.120 16 89746848 missense variant T/C;G snv 8.7E-05 2
rs587783028
FANCA
0.925 0.120 16 89752137 splice donor variant C/A;T snv 4.0E-06 2