Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112348497 1.000 0.080 21 43207769 intergenic variant -/C delins 0.20 1
rs199961668 1.000 0.080 7 471253 intergenic variant -/C delins 1
rs58788673 0.807 0.080 7 46864701 intergenic variant -/CA ins 0.22 7
rs3138869
AR
0.925 0.080 X 67546514 frameshift variant -/CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCG delins 2
rs879253799
DCAF17
0.882 0.320 2 171443559 frameshift variant A/- delins 5
rs201796065 1.000 0.080 2 176481554 intergenic variant A/- delins 1.2E-02 1
rs35534179
MTX2
1.000 0.080 2 176312686 intron variant A/- delins 1.6E-02 1
rs34991987
LOC105375343
0.807 0.080 7 69130240 downstream gene variant A/-;AA delins 7
rs34247753
TARDBP
1.000 0.080 1 11014942 intron variant A/-;AA delins 1
rs35689231
C2orf42
1.000 0.080 2 70185409 intron variant A/-;AA delins 0.43 1
rs6113491 0.925 0.080 20 22076777 downstream gene variant A/C snv 0.58 2
rs10516537
LOC105377356
1.000 0.080 4 106706914 intron variant A/C snv 0.84 1
rs56349397
HDAC9
1.000 0.080 7 18825739 intron variant A/C snv 0.28 1
rs690333 1.000 0.080 21 44752760 regulatory region variant A/C snv 0.47 1
rs745977 1.000 0.080 2 67854177 regulatory region variant A/C snv 0.51 1
rs9398035 1.000 0.080 6 105593507 downstream gene variant A/C snv 0.42 1
rs11243290
HULC ; LOC105374914
1.000 0.080 6 9000190 intron variant A/C;G snv 1
rs145226407 1.000 0.080 17 57154240 intergenic variant A/C;G snv 1
rs29073 1.000 0.080 18 9971793 regulatory region variant A/C;G snv 0.46 1
rs997683
TCF12
1.000 0.080 15 57249706 intron variant A/C;T snv 0.65 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs11593840
LRMDA
0.807 0.080 10 76436854 intron variant A/G snv 0.40 7
rs1160312
LINC01432
0.807 0.080 20 22069865 intron variant A/G snv 0.55 7
rs12083887 0.807 0.080 1 118339066 regulatory region variant A/G snv 0.62 7