Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 2
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 7
rs3811047
IL37
0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 1
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 12
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 18
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 3
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 6
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 7
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 2
rs16906252
MGMT
0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 2
rs2853669
TERT
0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 1
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 5
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 17
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 19
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 34
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 7
rs199769221
PRSS1
0.790 0.280 7 142751920 missense variant G/A;C;T snv 8.0E-05; 4.0E-06 1
rs2070803
TRIM46
0.925 0.080 1 155185239 intron variant G/A snv 0.55 2
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 7