Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs17007417 0.882 0.080 2 71808541 regulatory region variant T/C snv 0.85 3
rs12743824 0.925 0.040 1 99317401 intergenic variant C/A snv 0.48 2
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs940553638
ALDH2
0.827 0.200 12 111783222 missense variant G/A snv 1.6E-05 7.0E-06 6
rs1553403917
ALMS1
0.807 0.320 2 73451171 frameshift variant -/A delins 7
rs2854116
APOC3
0.807 0.200 11 116829453 upstream gene variant C/T snv 0.51 7
rs2070666
APOC3
0.882 0.120 11 116830958 intron variant T/A;C snv 4
rs74315468
ARSA
0.882 0.040 22 50626841 missense variant G/A snv 4.0E-06 2.8E-05 3
rs886041065
ASXL2
0.677 0.600 2 25743913 frameshift variant G/- delins 43
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs3213445
CHKB-CPT1B ; CPT1B
0.851 0.120 22 50577409 missense variant T/C snv 0.12 8.9E-02 4
rs12784396
CWF19L1
0.925 0.040 10 100267650 5 prime UTR variant C/A;T snv 4
rs1554888939
EHMT1
0.683 0.640 9 137798823 missense variant G/T snv 58
rs2862954
ERLIN1
0.925 0.040 10 100152307 missense variant T/C snv 0.34 0.32 2
rs2645424
FDFT1
0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8