Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006752
DTNB-AS1 ; DTNB
1.000 0.160 2 25441122 intron variant C/T snv 0.12 1
rs1016669
ULK4
1.000 0.160 3 41852948 intron variant T/C snv 0.32 1
rs10180663
DTNB
1.000 0.160 2 25410373 intron variant T/A;C;G snv 1
rs10212536
ULK4
1.000 0.160 3 41785534 intron variant A/C;G snv 1
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1025646
ULK4
1.000 0.160 3 41712930 intron variant A/T snv 0.26 1
rs1034447
LOC105378110
1.000 0.160 6 164192425 intergenic variant C/T snv 0.24 1
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10452020
ULK4
1.000 0.160 3 41774459 intron variant A/C;G snv 1
rs10452022
ULK4
1.000 0.160 3 41774550 intron variant G/A;C snv 1
rs1045433
TRNT1 ; CRBN
1.000 0.160 3 3149742 non coding transcript exon variant T/C snv 0.15 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10485986
DNAH11
1.000 0.160 7 21867059 intron variant C/T snv 0.32 1
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894231
LRRC56 ; HRAS
0.776 0.360 11 533467 missense variant C/G;T snv 9
rs104894340
CDK4
0.827 0.200 12 57751647 missense variant C/A;T snv 5
rs104894419
LIG4
0.807 0.360 13 108208829 stop gained G/A snv 9.9E-05 7.0E-05 8
rs1049623
DDR1
0.925 0.200 6 30897052 synonymous variant T/C snv 0.47 0.43 2
rs1049633
DDR1
1.000 0.160 6 30899750 3 prime UTR variant G/A snv 7.6E-02 1
rs10509328
LOC105378351
1.000 0.160 10 71007652 intron variant T/A;C snv 1
rs1050976
IRF4
0.851 0.280 6 408079 3 prime UTR variant C/T snv 0.37 4
rs10510729
ULK4
1.000 0.160 3 41790506 intron variant G/A snv 0.12 1