Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs568408
IL12A ; IL12A-AS1
0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
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
rs3020314
ESR1
0.790 0.280 6 151949537 intron variant C/G;T snv 7
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 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
rs1392080411
KLF2
0.827 0.160 19 16325934 missense variant C/T snv 7.0E-06 5
rs4937362
LOC105369568
0.827 0.240 11 128622844 intron variant T/C snv 0.49 5
rs6932542 0.827 0.200 6 32412485 downstream gene variant A/G snv 0.55 5
rs13254990
PVT1
0.882 0.120 8 128064205 intron variant C/T snv 0.24 4
rs2621416 0.882 0.280 6 32774091 intergenic variant T/C snv 0.26 4
rs4938573 0.851 0.280 11 118871133 regulatory region variant C/T snv 0.79 4
rs2857597
AIF1
0.882 0.200 6 31617223 upstream gene variant T/A snv 0.74 3
rs3115667 0.882 0.200 6 31675622 downstream gene variant T/A;C snv 0.74 3
rs3117222
HLA-DPA2
0.882 0.280 6 33093172 intron variant C/T snv 0.33 3
rs8094402
MBP
0.882 0.120 18 76995493 intron variant A/G snv 0.25 3
rs17749561 0.925 0.120 18 63115978 intergenic variant G/A snv 5.9E-02 2
rs2855429
COL11A2
0.925 0.120 6 33190412 intron variant A/C snv 0.78 2