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
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs4149584
TNFRSF1A
0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 24
rs28936375
CPT2
0.752 0.320 1 53197092 missense variant C/A snv 1.7E-04 2.2E-04 15
rs2348071
ARMH4 ; PSMA3
0.827 0.240 14 58263908 intron variant A/G snv 0.71 5
rs2295826
PSMC6
0.851 0.200 14 52708205 intron variant A/G snv 0.11 4
rs2295827
PSMC6
0.851 0.200 14 52708263 intron variant C/T snv 9.6E-02 9.1E-02 4
rs2277460
PSMA6
0.882 0.200 14 35292367 5 prime UTR variant C/A;T snv 3