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
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs1805015
IL4R
0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 17
rs1057519902
H3-3A
0.742 0.160 1 226064451 missense variant G/C snv 16
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv 14
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 7
rs2252586 0.882 0.040 7 54911231 intergenic variant C/T snv 0.27 5
rs1920116
LRRC31
0.882 0.040 3 169862183 intron variant G/A snv 0.25 5
rs117677079
ANXA5
0.882 0.040 4 121673909 intron variant T/C snv 8.3E-03 3
rs1805016
IL4R
0.882 0.080 16 27363606 missense variant T/G snv 6.4E-02 0.13 3
rs7502563
RPTOR
0.882 0.040 17 80947993 intron variant G/A snv 0.34 3