Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs138880920
ABCA1
1.000 0.040 9 104826957 missense variant C/G snv 3.3E-03 1.8E-03 1
rs33918808
ABCA1
1.000 0.040 9 104817351 missense variant C/G;T snv 3.5E-02; 4.0E-06 1
rs3917643
F3
1.000 0.040 1 94536311 intron variant T/C snv 3.9E-02 1
rs1740073 1.000 0.040 6 43979661 regulatory region variant T/C snv 0.67 2
rs2375981 1.000 0.040 9 2692583 regulatory region variant C/G;T snv 2
rs872129 0.925 0.080 1 203200263 intergenic variant A/G snv 0.19 2
rs750249283
ABCG1
0.925 0.080 21 42296256 missense variant C/G;T snv 4.0E-06; 8.0E-06 2
rs2293489
BUD23
0.925 0.120 7 73692949 non coding transcript exon variant C/T snv 0.26 2
rs17057255
EPHX2
0.925 0.080 8 27503724 missense variant C/T snv 1.3E-02 3.4E-02 2
rs281860391
HLA-B ; HLA-C
0.925 0.080 6 31271690 stop gained C/T snv 2
rs884164
PLIN4
0.925 0.040 19 4521613 upstream gene variant A/G;T snv 2
rs17105278
RAD51B
0.925 0.080 14 68261762 intron variant T/C snv 0.36 2
rs7043199
VLDLR ; VLDLR-AS1
1.000 0.040 9 2621145 intron variant T/A snv 0.18 2
rs2639990
ZADH2
1.000 0.040 18 75203596 intron variant T/C snv 0.12 2
rs1144507
ZNF202
0.925 0.080 11 123729767 missense variant A/C;G;T snv 0.68 2
rs4147929
ABCA7
0.882 0.120 19 1063444 intron variant A/C;G snv 3
rs12817819
ATP2B1
0.882 0.040 12 89645549 intron variant C/T snv 9.4E-02 3
rs4359426
CCL22
0.925 0.120 16 57358821 missense variant A/C;T snv 0.92 0.94 3
rs4782371
ZFPM1
1.000 0.040 16 88502423 intron variant T/A;G snv 3
rs10761741
JMJD1C
1.000 0.040 10 63306426 intron variant G/T snv 0.38 4
rs567798234
AMPD2
0.851 0.120 1 109625326 missense variant C/T snv 4.1E-06 7.0E-06 5
rs6749704
CCL20
0.827 0.240 2 227813126 intron variant T/C snv 0.24 5
rs114694170
MEF2C ; MEF2C-AS1
1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02 5
rs11234027
NADSYN1
0.882 0.080 11 71523061 intron variant G/A snv 0.24 5
rs2230808
ABCA1
0.827 0.240 9 104800523 missense variant T/C snv 0.71 0.60 6