Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11085754
SMARCA4
0.925 0.120 19 11017920 intron variant A/G snv 0.41 2
rs11644043
BRD7
0.925 0.120 16 50327466 intron variant T/C snv 0.24 2
rs1235228469
PIK3CB
0.925 0.120 3 138684714 missense variant C/A snv 8.0E-06 2
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 2
rs1276300653
CAMK1 ; OGG1
0.925 0.120 3 9757072 missense variant T/C snv 7.0E-06 2
rs12939944
MAP2K4
0.925 0.120 17 12056502 intron variant C/T snv 0.45 2
rs1318
LOC101928045 ; PITPNC1
0.925 0.120 17 67695266 3 prime UTR variant A/G snv 0.30 2
rs13303010
KLHL17 ; NOC2L
0.925 0.120 1 959193 intron variant G/A snv 0.82 0.69 2
rs1336539869
CDK4
0.925 0.120 12 57751681 missense variant C/G snv 2
rs1339638227
CDKN2A
0.925 0.120 9 21971119 missense variant T/C snv 4.3E-06 2
rs138147246
OGG1
0.925 0.120 3 9756551 synonymous variant A/G snv 8.0E-06 1.4E-05 2
rs139632793
OGG1
0.925 0.120 3 9751114 missense variant G/C snv 5.2E-05 1.7E-04 2
rs141095230
MGMT
0.925 0.120 10 129536277 missense variant C/A;T snv 8.0E-06; 5.2E-05 2
rs1412335442
PIK3CG
0.925 0.120 7 106868317 missense variant G/T snv 7.0E-06 2
rs1448106115
PMS2
0.925 0.120 7 5989944 missense variant T/C snv 4.0E-06 2
rs145574072
OGG1
0.925 0.120 3 9754765 synonymous variant T/C snv 4.0E-06 2
rs145733073
UGT1A8 ; UGT1A9 ; UGT1A7 ; UGT1A10
0.925 0.120 2 233682175 missense variant T/C;G snv 4.0E-06; 1.4E-04 2
rs149243735
OGG1
0.925 0.120 3 9751076 missense variant C/A snv 4.0E-06 2
rs1517037 0.882 0.120 18 59211042 intergenic variant C/T snv 0.23 2
rs1537373
CDKN2B-AS1
0.925 0.120 9 22103342 intron variant T/G snv 0.63 2
rs1552462 0.925 0.120 11 7235910 upstream gene variant C/T snv 2.7E-02 2
rs1630747
SLC5A3 ; MRPS6
0.925 0.120 21 34085692 intron variant C/A snv 0.69 2
rs17458086
SLC2A13
0.925 0.120 12 40034837 intron variant T/C snv 1.1E-02 2
rs17884306
TP53
0.925 0.120 17 7668783 3 prime UTR variant C/T snv 5.1E-02 2
rs1800843
CCKBR
0.925 0.120 11 6270835 synonymous variant C/A;G snv 0.16; 4.0E-06 0.19 2