Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2546191
ELL2
0.851 0.160 5 95896837 intron variant G/A snv 0.38 4
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1057035
DICER1
0.763 0.440 14 95087805 3 prime UTR variant T/C snv 0.26 12
rs4406737
FAS
0.925 0.120 10 88999967 intron variant A/G snv 0.50 2
rs2147420
FAS
1.000 0.120 10 88999856 intron variant A/G snv 0.50 1
rs6586163
FAS ; FAS-AS1 ; ACTA2
0.925 0.120 10 88992261 non coding transcript exon variant A/C snv 0.58 2
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2266690
CCNH
1.000 0.120 5 87399457 missense variant A/G;T snv 1
rs4240807 0.851 0.160 16 85951755 downstream gene variant A/C snv 0.76 4
rs305061 0.851 0.280 16 85942053 intron variant C/A;T snv 4
rs1044873
IRF8
0.925 0.120 16 85922065 3 prime UTR variant C/T snv 0.40 2
rs2292982
IRF8
1.000 0.120 16 85911217 intron variant T/C;G snv 3
rs391525
IRF8
0.882 0.200 16 85910833 intron variant A/G;T snv 0.35 3
rs391855 0.925 0.120 16 85895015 upstream gene variant A/T snv 0.52 2
rs391023 0.925 0.120 16 85894208 upstream gene variant C/T snv 0.48 2
rs783540
CPEB1
0.925 0.160 15 82585958 intron variant A/G;T snv 2
rs1057519832
PLCG2
1.000 0.120 16 81928578 missense variant A/C;G;T snv 1
rs1057519831
PLCG2
1.000 0.120 16 81912655 missense variant C/T snv 3
rs4505265
IL16
1.000 0.120 15 81185114 intron variant A/C snv 1
rs1642785
TP53
0.807 0.200 17 7676483 5 prime UTR variant G/A;C;T snv 1.2E-05; 0.67; 2.8E-05 6