Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1005734
LOC105376878 ; RUNX3
1.000 0.080 1 24935531 intron variant C/A;T snv 1
rs10193725
WNT6
1.000 0.080 2 218861775 intron variant T/C snv 0.37 1
rs10225279
TWIST1
1.000 0.080 7 19093449 intron variant G/T snv 0.57 1
rs10278449
HDAC9-AS1 ; HDAC9
1.000 0.080 7 18891596 intron variant C/T snv 0.74 1
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs10502861
SLC14A2
0.807 0.080 18 45220183 intron variant C/T snv 0.32 7
rs10516537
LOC105377356
1.000 0.080 4 106706914 intron variant A/C snv 0.84 1
rs1057517491
GJB2
0.776 0.240 13 20189448 frameshift variant C/- delins 8
rs10771462 1.000 0.080 12 29004395 intergenic variant G/A snv 0.82 1
rs10808813
ZFHX4-AS1
1.000 0.080 8 76604707 intron variant C/G;T snv 1
rs1081073
EBF1
1.000 0.080 5 158954504 intron variant T/A snv 0.39 1
rs10843003 1.000 0.080 12 27834007 intergenic variant T/G snv 0.14 1
rs10888690
FAF1
0.807 0.080 1 50494849 intron variant T/A;C snv 7
rs10903128 1.000 0.080 1 25036847 upstream gene variant A/G snv 0.68 1
rs10919382 1.000 0.080 1 170392023 intergenic variant A/G snv 0.36 1
rs10928235
TEX41
1.000 0.080 2 144920547 intron variant A/T snv 0.18 2
rs10930758 0.807 0.080 2 176897100 intergenic variant A/G;T snv 7
rs11037975 0.807 0.080 11 44389312 intergenic variant C/A;G snv 7
rs11049231 1.000 0.080 12 27938767 upstream gene variant G/A snv 4.6E-02 1
rs111238176
FASLG
0.851 0.160 1 172665840 missense variant A/G snv 4
rs111668293
TBX15
0.807 0.080 1 118896200 intron variant G/- del 0.12 7
rs111810219
ARHGEF9
1.000 0.080 X 63717947 intron variant G/A snv 2.3E-02 1
rs112069404 1.000 0.080 X 66331306 intergenic variant C/A;T snv 1
rs11220486
ST3GAL4
1.000 0.080 11 126421126 intron variant G/A snv 0.19 1
rs112348497 1.000 0.080 21 43207769 intergenic variant -/C delins 0.20 1