Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs20576
TNFRSF10A
0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs2511714 0.925 0.120 8 102566646 regulatory region variant T/G snv 0.41 2
rs7944004 0.925 0.120 11 2289922 intergenic variant T/G snv 0.48 2
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs3803185
ARL11
0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 19
rs6793295
LRRC34
0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 6
rs13397985
SP110 ; SP140
0.827 0.280 2 230226508 intron variant T/C;G snv 5
rs754688962
SF3B1
0.851 0.200 2 197402637 missense variant T/C;G snv 5
rs2292982
IRF8
1.000 0.120 16 85911217 intron variant T/C;G snv 3
rs7578199
HDLBP
0.925 0.120 2 241253433 missense variant T/C;G snv 0.19; 8.4E-05 2
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs758272654
GNAS
0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs1057035
DICER1
0.763 0.440 14 95087805 3 prime UTR variant T/C snv 0.26 12
rs301
LPL
0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 7
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 6
rs181181503
LOC100507377
0.851 0.160 12 74276187 intron variant T/C snv 1.5E-03 4
rs6763508
ULK4
0.851 0.160 3 41709497 intron variant T/C snv 0.30 4
rs210142
GGNBP1 ; BAK1
0.925 0.120 6 33579060 intron variant T/C snv 0.74 3