Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10416839 1.000 0.040 19 41776424 intron variant G/T snv 0.26 1
rs11133504 1.000 0.040 4 57514156 intergenic variant G/A snv 0.23 1
rs11739663 1.000 0.040 5 593968 intergenic variant T/C snv 0.29 1
rs13337840 1.000 0.040 16 86793733 intergenic variant A/G snv 0.28 1
rs16940186 1.000 0.040 16 85976134 intron variant T/C snv 0.17 1
rs17771967 1.000 0.040 19 54868759 downstream gene variant A/G snv 0.42 1
rs1830610 1.000 0.040 9 5260079 intergenic variant C/G;T snv 1
rs2457996 1.000 0.040 4 73990818 upstream gene variant C/A;G;T snv 1
rs2764742 1.000 0.040 16 20019510 intergenic variant C/A;T snv 1
rs4510766 1.000 0.040 7 107852344 intergenic variant A/G snv 0.36 1
rs4722672 1.000 0.040 7 27192143 intron variant C/T snv 0.73 1
rs6437358 1.000 0.040 2 240657733 intergenic variant G/C snv 0.33 1
rs6451493 1.000 0.040 5 40410833 upstream gene variant G/A;T snv 1
rs6951457 1.000 0.040 7 107815875 intergenic variant G/A;C snv 1
rs7911117 1.000 0.040 10 26890667 regulatory region variant T/G snv 0.18 1
rs886774 1.000 0.040 7 107854989 regulatory region variant G/A snv 0.67 1
rs9271209 1.000 0.040 6 32611258 intergenic variant G/A snv 0.74 1
rs943072 1.000 0.040 6 43828231 intron variant G/T snv 0.83 1
rs9548988 1.000 0.040 13 39931373 regulatory region variant C/T snv 0.44 1
rs3740415
ACTR1A ; MFSD13A
1.000 0.040 10 102472959 3 prime UTR variant G/A snv 0.48 0.48 1
rs4725479
ACTR3B
1.000 0.040 7 153048725 intergenic variant T/C snv 0.64 1
rs2241877
ATG16L1
1.000 0.040 2 233277843 intron variant A/G snv 0.69 1
rs6911490
ATG5 ; PRDM1
1.000 0.040 6 106074152 intron variant T/C snv 0.86 1
rs41417449
BTNL2 ; TSBP1-AS1
1.000 0.040 6 32396234 missense variant T/C snv 2.3E-02 9.5E-03 1
rs254562
C5orf66
1.000 0.040 5 135105767 intron variant A/G snv 0.32 1