Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11719165 0.925 0.040 3 194865359 intergenic variant T/C snv 0.53 2
rs12046844 0.925 0.040 1 65772696 regulatory region variant G/A snv 0.17 2
rs1901440 0.925 0.040 2 133680388 intergenic variant C/A snv 0.58 2
rs7091672 0.925 0.040 10 118836909 intron variant T/A;C;G snv 2
rs12720066
ABCB1
0.925 0.040 7 87540386 intron variant A/C snv 3.9E-02 2
rs1260186456
ABCC1
0.925 0.040 16 16102659 missense variant G/T snv 9.4E-06 2
rs17501331
ABCC1
0.925 0.040 16 15995584 intron variant A/G snv 7.7E-02 2
rs1885301
ABCC2
0.925 0.040 10 99781296 upstream gene variant A/G snv 0.58 2
rs4148396
ABCC2
0.925 0.040 10 99832187 intron variant T/C snv 0.65 2
rs10824095
ADK
0.925 0.040 10 74176853 5 prime UTR variant C/G;T snv 0.67 2
rs7608692
CASP8
0.925 0.040 2 201246236 intron variant G/A snv 0.20 2
rs7761731
CYP39A1
0.925 0.040 6 46596080 missense variant A/G;T snv 0.35 2
rs9990999
DCTD
0.925 0.040 4 182902820 intron variant G/A snv 0.37 2
rs1482105290
DLEU2 ; TRIM13
0.925 0.040 13 50012772 missense variant A/G snv 4.0E-06 2
rs546229463
FCGR3B
0.925 0.040 1 161629912 missense variant T/C snv 2
rs1422359334
GSTK1 ; LOC105375545
0.925 0.040 7 143264131 missense variant C/A;T snv 4.0E-06 2
rs1610696
HLA-G
0.925 0.040 6 29831026 3 prime UTR variant C/G snv 0.29 2
rs6498588
LOC107984869
0.925 0.040 16 15938949 intergenic variant A/T snv 0.65 2
rs12934241
MMP2
0.925 0.040 16 55486666 non coding transcript exon variant C/G;T snv 2
rs3136228
MSH6
0.925 0.040 2 47782677 intron variant T/G snv 0.30 2
rs3087403
REV1
0.925 0.040 2 99442408 missense variant C/T snv 0.28 0.28 2
rs1424665740
SLC10A2
0.925 0.040 13 103066068 missense variant T/C snv 4.0E-06 7.0E-06 2
rs3825876
SLC28A1
0.925 0.040 15 84892637 intron variant G/A snv 0.34 2
rs693955
SLC29A1
0.925 0.040 6 44224183 intron variant A/C snv 0.85 2
rs747199
SLC29A1
0.925 0.040 6 44226608 intron variant G/C snv 0.15 2