Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9815354
ULK4
0.925 0.160 3 41871159 intron variant G/A;T snv 4
rs138740
TOM1
0.882 0.160 22 35303589 intron variant C/T snv 0.51 3
rs1716983
ULK4
1.000 0.160 3 41922636 intron variant G/A;C;T snv 3
rs1717027
ULK4
1.000 0.160 3 41946428 intron variant T/A;C snv 3
rs34562254
TNFRSF13B
1.000 0.160 17 16939677 missense variant G/A snv 0.14 0.12 3
rs56219066
ELL2
0.882 0.160 5 95907227 intron variant T/A;C snv 3
rs57104699
DNAH11
0.882 0.160 7 21888461 intron variant C/A snv 0.26 3
rs57968458 0.882 0.160 17 16916785 intergenic variant G/A snv 0.15 3
rs6919908
USP8P1 ; HLA-B
0.882 0.160 6 31277183 non coding transcript exon variant T/C snv 0.83 3
rs73071352
ULK4
0.882 0.160 3 41786808 intron variant A/G snv 0.12 3
rs73081364
ULK4
1.000 0.160 3 41872124 intron variant G/A;C;T snv 3
rs7622665
ULK4
1.000 0.160 3 41929251 intron variant T/C snv 0.67 3
rs879882
POU5F1
1.000 0.160 6 31171675 intron variant T/C;G snv 3
rs9848754
ULK4
0.882 0.160 3 41712155 intron variant C/T snv 0.18 3
rs1052501
ULK4
0.925 0.160 3 41883906 missense variant C/G;T snv 0.80 2
rs1057519718
BRAF
0.925 0.160 7 140753355 missense variant CA/TC mnv 2
rs10936601
LRRC34
1.000 0.160 3 169810661 intron variant C/T snv 0.37 2
rs12630450 1.000 0.160 3 169762416 downstream gene variant A/G snv 0.33 2
rs12717
TBP ; PSMB1
0.925 0.160 6 170553212 missense variant G/C snv 0.42 0.38 2
rs2272007
ULK4
1.000 0.160 3 41954644 missense variant T/C snv 0.79 0.67 2
rs2285803
PSORS1C2 ; PSORS1C1
0.925 0.160 6 31139481 intron variant T/C snv 0.72 2
rs2683696
ULK4
1.000 0.160 3 41873406 intron variant T/C snv 0.34 2
rs28581706
ULK4
1.000 0.160 3 41829905 intron variant A/C;T snv 2
rs3821383
MYNN
1.000 0.160 3 169772158 upstream gene variant A/C;G;T snv 2
rs62258655
ULK4
1.000 0.160 3 41890838 intron variant G/A snv 0.11 2