Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8187710
ABCC2
0.827 0.200 10 99851537 missense variant G/A snv 5.3E-02 8.5E-02 6
rs17222723
ABCC2
0.925 0.080 10 99836239 missense variant T/A snv 4.5E-02 5.5E-02 2
rs781469754
MTTP
1.000 0.040 4 99591691 missense variant A/G snv 4.0E-06 7.0E-06 1
rs3805335
MTTP
1.000 0.040 4 99586478 intron variant C/T snv 1.3E-02 1
rs1057613
MTTP
1.000 0.040 4 99583828 3 prime UTR variant G/A snv 0.60 1
rs3816873
MTTP
0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 9
rs2306986
MTTP
1.000 0.040 4 99583418 missense variant G/C;T snv 5.9E-02 1
rs61733139
MTTP
1.000 0.040 4 99583409 missense variant G/C snv 4.0E-02 4.9E-02 1
rs1412189378
MTTP
1.000 0.040 4 99583404 missense variant C/A snv 1
rs756998920
MTTP
1.000 0.040 4 99581967 missense variant G/A snv 3.4E-04 8.4E-05 1
rs1800804
MTTP
1.000 0.040 4 99574660 intron variant T/C snv 0.26 1
rs1800591
MTTP
0.882 0.120 4 99574331 intron variant G/T snv 0.26 3
rs139271658
PTPRD
1.000 0.040 9 9797383 intron variant A/G snv 1.9E-02 2
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs4240624
LOC157273
0.882 0.040 8 9326721 intron variant G/A snv 0.87 5
rs6487679 0.925 0.080 12 9218736 intergenic variant C/T snv 0.80 2
rs61756425
PPP1R3B
1.000 0.040 8 9141529 missense variant G/T snv 1.6E-02 1.0E-02 1
rs72943235 1.000 0.040 2 88201127 intergenic variant G/A snv 9.0E-02 1
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs72613567
HSD17B13
0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs35929428
PTPRD
1.000 0.040 9 8485834 missense variant G/A;C snv 9.2E-02; 4.0E-06 1
rs1805074
DMGDH
1.000 0.040 5 79028529 missense variant A/G snv 0.27 0.33 1
rs11235972
UCP3
1.000 0.040 11 74006029 intron variant G/A snv 0.21 1
rs659366
UCP2
0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17