Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs1626340 0.827 0.120 9 99161090 intergenic variant G/A;T snv 5
rs72802342 0.851 0.040 16 75200974 downstream gene variant C/A snv 6.2E-02 5
rs10781182 0.851 0.040 9 74002804 intergenic variant T/G snv 0.54 4
rs114092250 0.851 0.040 5 35494346 intergenic variant G/A;T snv 4
rs142450006 0.851 0.040 20 45986353 regulatory region variant TTCT/-;TTCTTTCT delins 2.0E-02 4
rs148553336 0.851 0.040 1 196644043 intergenic variant T/C snv 7.7E-03 4
rs201459901 0.851 0.040 20 58078668 regulatory region variant -/A delins 0.21 4
rs61818925 0.851 0.040 1 196846320 upstream gene variant T/G snv 0.67 4
rs28368872 0.882 0.040 16 10491493 upstream gene variant G/A snv 0.22 3
rs4482537 0.925 0.040 2 48825116 intron variant C/T snv 0.52 2
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs225396
ABCG1
0.925 0.040 21 42267244 intron variant C/T snv 0.45 2
rs57137919
ABCG1 ; LOC105372814
0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs61941274
ACAD10
0.827 0.160 12 111694806 intron variant G/A;T snv 5
rs62247658
ADAMTS9-AS2
0.851 0.040 3 64729479 intron variant C/T snv 0.42 4
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 9
rs11775442
ANGPT2 ; MCPH1
0.925 0.040 8 6538837 intron variant A/G snv 0.20 2
rs13269021
ANGPT2 ; MCPH1
0.925 0.040 8 6539242 intron variant G/A;T snv 2
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs12357257
ARHGAP21
0.851 0.040 10 24710664 intron variant G/A snv 0.18 4
rs10490924
ARMS2 ; LOC105378525
0.716 0.240 10 122454932 missense variant G/T snv 0.26 0.23 16
rs3750846
ARMS2 ; LOC105378525
0.851 0.040 10 122456049 intron variant T/C snv 0.24 4
rs2736911
ARMS2 ; LOC105378525
0.882 0.120 10 122454839 stop gained C/A;T snv 4.0E-06; 0.13 3