Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10919791 0.925 0.240 1 199996040 intergenic variant G/A snv 0.22 1
rs2816938 1.000 0.120 1 200016240 upstream gene variant T/A snv 0.37 1
rs9363918 0.882 0.200 6 68432116 intron variant T/G snv 0.38 1
rs10094872
CASC11
0.882 0.200 8 127707639 intron variant A/T snv 0.33 1
rs372266620
CDKN2A
0.925 0.120 9 21971189 missense variant G/A;C;T snv 9.1E-05; 2.3E-05; 9.1E-06 1
rs4269383
LOC105378072 ; LOC101928923
0.882 0.120 6 155876368 intergenic variant A/G snv 0.37 1
rs876493
PNMT
0.925 0.160 17 39668292 intron variant G/A snv 0.47 1
rs375328708
STK11
1.000 0.120 19 1226602 synonymous variant C/G;T snv 6.7E-05 6.3E-05 1
rs35226131
TERT
1.000 0.120 5 1295258 upstream gene variant C/T snv 2.6E-02 1
rs9854771
TP63
0.925 0.240 3 189790682 intron variant G/A snv 0.34 1
rs10887710 0.925 0.120 10 80270029 downstream gene variant T/C snv 0.19 2
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 2
rs1517037 0.882 0.120 18 59211042 intergenic variant C/T snv 0.23 2
rs1552462 0.925 0.120 11 7235910 upstream gene variant C/T snv 2.7E-02 2
rs2980879 0.925 0.120 8 125469233 intron variant A/T snv 0.69 2
rs6001516 0.925 0.120 22 39248198 intron variant C/T snv 6.1E-02 2
rs11644043
BRD7
0.925 0.120 16 50327466 intron variant T/C snv 0.24 2
rs782128510
C17orf97 ; LOC105371430
0.925 0.120 17 410373 missense variant C/A;G snv 7.6E-05; 8.4E-06 2
rs1276300653
CAMK1 ; OGG1
0.925 0.120 3 9757072 missense variant T/C snv 7.0E-06 2
rs1800843
CCKBR
0.925 0.120 11 6270835 synonymous variant C/A;G snv 0.16; 4.0E-06 0.19 2
rs1336539869
CDK4
0.925 0.120 12 57751681 missense variant C/G snv 2
rs2206734
CDKAL1
0.882 0.160 6 20694653 intron variant C/T snv 0.20 2
rs1339638227
CDKN2A
0.925 0.120 9 21971119 missense variant T/C snv 4.3E-06 2
rs1537373
CDKN2B-AS1
0.925 0.120 9 22103342 intron variant T/G snv 0.63 2
rs6475609
CDKN2B-AS1
0.925 0.120 9 22106272 intron variant A/C;G;T snv 2