Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
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
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 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
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 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
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16