Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11020802
ANKRD49 ; MRE11
0.882 0.080 11 94493959 upstream gene variant C/A;G;T snv 3
rs1060503291
APC
0.882 0.080 5 112835135 missense variant C/T snv 3
rs140920401
ARAF
0.882 0.080 X 47563284 missense variant G/A snv 3
rs868188
ARHGEF11 ; MIR765 ; LRRC71
0.882 0.080 1 156937323 missense variant T/C snv 0.40 0.33 3
rs807185
ATG4A
0.882 0.080 X 108097488 intron variant A/T snv 3
rs11212592
ATM ; C11orf65
0.882 0.080 11 108348120 intron variant A/G snv 0.16 3
rs3866958
B9D1 ; MAPK7
0.882 0.080 17 19377693 intron variant A/C;T snv 0.89 3
rs575508709
BAG6
0.882 0.080 6 31649333 missense variant C/G snv 4.0E-06 3
rs7501331
BCO1
0.882 0.080 16 81280891 missense variant C/T snv 0.21 0.18 3
rs6141383
BPIFB1
0.882 0.080 20 33301335 missense variant G/A snv 1.7E-03 9.9E-04 3
rs868021367
BRAF
0.882 0.080 7 140753319 missense variant C/G snv 3
rs756402191
C10orf55 ; PLAU
0.882 0.080 10 73913605 missense variant G/A;T snv 1.2E-04; 4.0E-05 3
rs652311
C11orf65 ; ATM
0.882 0.080 11 108369342 intron variant G/A snv 0.54 3
rs16832404
C2orf88
0.882 0.080 2 190188403 intron variant T/C snv 0.12 3
rs507879
CASP5
0.882 0.080 11 105007200 missense variant T/A;C;G snv 0.43 0.49 3
rs1410508127
CASP7
0.882 0.080 10 113679831 missense variant A/C;G snv 3
rs1422012687
CASP9
0.882 0.080 1 15524124 stop gained C/A;T snv 7.2E-06; 7.2E-06 3
rs1049337
CAV1
0.882 0.080 7 116560533 3 prime UTR variant C/T snv 0.25 3
rs2977549
CCN4
0.882 0.080 8 133229790 3 prime UTR variant C/A;T snv 3
rs3739262
CCN4
0.882 0.080 8 133193470 intron variant G/A snv 0.24 3
rs754958
CCN4
0.882 0.080 8 133226528 intron variant G/A;T snv 3
rs769236
CCNA2 ; BBS7
0.882 0.080 4 121823883 5 prime UTR variant C/A;T snv 3
rs2282987
CDK6
0.882 0.080 7 92683489 intron variant G/C snv 3.7E-02 3
rs10487372
CFTR ; CFTR-AS1
0.882 0.080 7 117560845 intron variant C/T snv 0.13 3
rs876659871
CHEK2
0.882 0.080 22 28719462 missense variant C/T snv 7.0E-06 3