Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs78311289
FGFR3
0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 25
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 17
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41 12
rs121913514
KIT
0.763 0.240 4 54733174 missense variant T/A;G snv 12
rs995030
KITLG
0.776 0.320 12 88496894 3 prime UTR variant A/G snv 0.67 9
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 7
rs755383
DMRT1
0.807 0.120 9 863635 intron variant C/T snv 0.54 7
rs2900333
ATF7IP
0.882 0.200 12 14500933 3 prime UTR variant C/A;G;T snv 6
rs2075789
MSH5-SAPCD1 ; LOC105375020 ; MSH5
0.882 0.120 6 31740551 missense variant C/T snv 0.13 9.1E-02 6
rs1508595 0.851 0.240 12 88592239 intron variant G/A;T snv 5
rs4624820 0.851 0.240 5 142302223 regulatory region variant G/A snv 0.55 5
rs210138
GGNBP1 ; BAK1
0.851 0.240 6 33574761 intron variant A/G snv 0.19 5
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs7040024
DMRT1
0.925 0.120 9 845516 intron variant A/C;G snv 4
rs3782181
KITLG
0.882 0.120 12 88559784 intron variant C/A snv 0.65 4
rs6060373
UQCC1
0.925 0.200 20 35326405 intron variant A/G snv 0.49 4
rs4699052 0.925 0.200 4 103216633 intergenic variant C/T snv 0.44 3
rs12435857
ESR2
0.925 0.200 14 64256807 intron variant G/A snv 0.41 3
rs2978381
ESR2
0.925 0.160 14 64299934 intron variant T/C snv 0.53 3
rs1355972653
IFNGR2
0.882 0.120 21 33415009 synonymous variant G/A snv 4.0E-06 7.0E-06 3