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
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15 8
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 7
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 7
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs4937362
LOC105369568
0.827 0.240 11 128622844 intron variant T/C snv 0.49 5
rs4938573 0.851 0.280 11 118871133 regulatory region variant C/T snv 0.79 4
rs13254990
PVT1
0.882 0.120 8 128064205 intron variant C/T snv 0.24 4
rs17749561 0.925 0.120 18 63115978 intergenic variant G/A snv 5.9E-02 2
rs2681416
CD86
0.925 0.120 3 122098766 intron variant G/A snv 0.26 2
rs6444305
LPP
0.925 0.120 3 188582114 intron variant G/A;C;T snv 2
rs12195582 1.000 0.120 6 32476767 upstream gene variant C/T snv 0.39 1
rs3751913
CYBC1
1.000 0.120 17 82447676 non coding transcript exon variant T/C snv 0.19 0.19 1
rs11082438
SLC14A2
1.000 0.120 18 45285245 intron variant G/T snv 8.3E-02 1