Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4149339
ABCA1
1.000 0.040 9 104782875 3 prime UTR variant G/A snv 0.32 2
rs2230808
ABCA1
0.827 0.240 9 104800523 missense variant T/C snv 0.71 0.60 6
rs4743763
ABCA1
1.000 0.040 9 104830901 intron variant A/C;T snv 0.36 2
rs2472386
ABCA1
1.000 0.040 9 104839260 intron variant G/A snv 0.47 3
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs11066782
KCTD10
1.000 0.040 12 109472747 intron variant C/T snv 0.17 2
rs11613718
KCTD10
1.000 0.040 12 109474527 intron variant C/T snv 0.17 2
rs11067233
MMAB
1.000 0.040 12 109556403 3 prime UTR variant C/G snv 0.23 0.24 2
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs730882082
LDLR
0.882 0.080 19 11105315 missense variant G/A;T snv 1.6E-05 5
rs879254535
LDLR
0.925 0.080 19 11105369 missense variant T/A;C;G snv 5
rs1057519655
LDLR
1.000 0.080 19 11105516 missense variant T/C;G snv 4.0E-06 2
rs730882087
LDLR
19 11106640 missense variant GG/AC mnv 1
rs544453230
LDLR
0.882 0.080 19 11110714 missense variant G/A;C snv 2.8E-05; 4.0E-06 6
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs11774572 1.000 0.040 8 11589291 regulatory region variant C/G;T snv 2
rs10488699
BUD13
11 116761784 intron variant C/T snv 1.0E-01 1
rs10488698
BUD13
1.000 0.040 11 116763231 missense variant G/A snv 6.4E-02 4.8E-02 2
rs2187126
BUD13
11 116765068 intron variant A/G snv 4.8E-02 2
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs2075294
ZPR1
11 116787406 intron variant G/T snv 3.5E-02 1
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15