Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs2276109
MMP12
0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 18
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs1801252
ADRB1
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs1805127
KCNE1
0.732 0.240 21 34449523 missense variant T/C snv 0.64 2.0E-04 17
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs1022113606
SOD3
0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16