Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5768709
TAFA5
0.925 0.120 22 48533757 intron variant A/G snv 0.36 2
rs4927850
TFRC
0.925 0.120 3 196024759 intron variant T/C snv 0.71 2
rs78417682
TNS3
0.925 0.120 7 47449305 intron variant G/C snv 0.15 2
rs17884306
TP53
0.925 0.120 17 7668783 3 prime UTR variant C/T snv 5.1E-02 2
rs935821839
TP73
0.925 0.120 1 3727199 missense variant A/G snv 7.0E-06 2
rs949647240
TP73
0.925 0.120 1 3707693 missense variant C/T snv 2
rs7074891
TRDMT1
0.925 0.120 10 17146475 3 prime UTR variant C/T snv 0.95 2
rs2980874
TRIB1
0.925 0.120 8 125432546 intron variant G/A snv 0.30 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
rs3729587
XPC
0.925 0.120 3 14167125 intron variant G/C snv 0.31 0.34 2
rs3731114
XPC
0.925 0.120 3 14165122 intron variant C/G snv 1.8E-02 2
rs2470353
XPC ; LOC107986063
0.925 0.120 3 14148768 intron variant G/A;C;T snv 0.41; 1.5E-04 2
rs3731055
XPC ; LSM3
0.925 0.120 3 14178939 intron variant C/T snv 1.9E-02 2
rs12029406 0.882 0.120 1 199936700 intergenic variant C/T snv 0.36 3
rs1517037 0.882 0.120 18 59211042 intergenic variant C/T snv 0.23 3
rs2980879 0.925 0.120 8 125469233 intron variant A/T snv 0.69 3
rs7503953 0.882 0.320 17 6238357 intergenic variant A/C snv 0.81 3
rs9363918 0.882 0.200 6 68432116 intron variant T/G snv 0.38 3
rs9543325 0.882 0.200 13 73342491 regulatory region variant C/G;T snv 3
rs150495372
ADH1B
0.925 0.120 4 99313834 missense variant C/T snv 3.7E-04 3
rs1209809979
AKR1A1
0.925 0.120 1 45568989 missense variant A/G snv 4.0E-06 3
rs2027605
BACH1
1.000 0.120 21 29354452 intron variant A/G snv 0.48 3
rs397507851
BRCA2
0.925 0.120 13 32340761 frameshift variant AAATGTT/- delins 3
rs1537373
CDKN2B-AS1
0.925 0.120 9 22103342 intron variant T/G snv 0.63 3
rs2762932
CYP24A1
0.882 0.200 20 54151852 downstream gene variant T/C snv 0.17 3