Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12732894
ARHGEF10L
0.882 0.080 1 17582733 intron variant G/A snv 1.6E-02 3
rs2244444
ARHGEF10L
0.882 0.080 1 17520426 intergenic variant C/T snv 0.55 3
rs779555087
HNF4A
0.882 0.080 20 44414561 missense variant A/G snv 1.6E-05 1.4E-05 3
rs1476081557
KMT2B
0.882 0.080 19 35721455 missense variant G/T snv 7.0E-06 3
rs764555290
KRT6A
0.882 0.080 12 52492759 missense variant G/C snv 1.2E-05 1.4E-05 3
rs230496
NFKB1
0.882 0.080 4 102567334 intron variant G/A snv 0.59 3
rs3811741
PLK4
0.882 0.080 4 127882004 intron variant G/A snv 0.74 3
rs745501336
RAB43 ; ISY1-RAB43
0.882 0.080 3 129091263 missense variant C/T snv 4.6E-05 7.0E-06 3
rs587782237
TP53
0.882 0.080 17 7670637 missense variant C/T snv 3
rs1330010954
DLC1
0.882 0.080 8 13094897 missense variant C/T snv 4.0E-06 4
rs372894000
DLC1
0.882 0.080 8 13092766 missense variant C/T snv 2.0E-05 1.4E-05 4
rs756966085
DLC1
0.882 0.080 8 13090431 missense variant C/T snv 8.0E-06 7.0E-06 4
rs763569821
MUC1
0.851 0.160 1 155188197 missense variant T/C snv 1.2E-05 4
rs230525
NFKB1
0.882 0.080 4 102537720 non coding transcript exon variant G/A snv 0.69 4
rs230530
NFKB1
0.882 0.080 4 102532823 intron variant A/G snv 0.37 4
rs1234220
PTEN
0.851 0.080 10 87885716 intron variant A/G snv 9.1E-02 4
rs769031989
STAT3
0.851 0.160 17 42322464 missense variant T/A snv 7.0E-06 4
rs2241715
TGFB1
0.851 0.120 19 41350981 5 prime UTR variant A/C snv 0.68 4
rs80309960
XRCC5
0.851 0.080 2 216122110 missense variant T/A snv 3.5E-04 1.1E-03 4
rs843645
ACYP2
0.827 0.120 2 54247527 intron variant T/A;G snv 0.19 5
rs5854292
EGFEM1P
0.851 0.080 3 168680960 intron variant AA/-;A;AAA delins 5
rs2299939
PTEN
0.827 0.080 10 87897393 intron variant C/A;T snv 5
rs1051861187
ABCB4
0.827 0.080 7 87409385 missense variant A/G snv 6
rs843706
ACYP2 ; TSPYL6
0.807 0.160 2 54253232 3 prime UTR variant C/A snv 0.42 6
rs867384693
HDAC3
0.851 0.120 5 141625349 missense variant C/A;T snv 6