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
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs1564045331
XPA
0.716 0.320 9 97687208 inframe deletion ATTCTT/- delins 35
rs778543124
XPA
0.716 0.320 9 97675476 frameshift variant AGTCTTACGGTACA/- delins 6.8E-05 6.3E-05 35
rs1393350
LOC107984363 ; TYR
0.851 0.160 11 89277878 intron variant G/A snv 0.17 7
rs7208422
TMC8
0.807 0.120 17 78134494 missense variant A/C;T snv 4.0E-06; 0.51 6
rs7164132
KNSTRN
0.925 0.080 15 40382954 missense variant C/A snv 9.2E-02 8.9E-02 2
rs139810560 1.000 0.080 16 89945331 upstream gene variant C/A snv 5.1E-02 1
rs773553186
TP53
1.000 0.080 17 7670636 missense variant T/A snv 2.0E-05 2.1E-05 1