Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2965667 0.776 0.080 12 17291799 intergenic variant A/T snv 0.96 10
rs209489
ELOVL5
0.790 0.080 6 53312880 intron variant C/A snv 0.92 9
rs7229639
SMAD7
0.763 0.080 18 48924606 intron variant A/G snv 0.87 13
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85 11
rs10849432
LOC105369625
0.790 0.080 12 6276561 intergenic variant C/T snv 0.84 9
rs4378954
LSAMP
0.790 0.080 3 115931601 intron variant T/C snv 0.83 10
rs13831
GNAS
0.790 0.080 20 58900136 3 prime UTR variant A/G snv 0.77 9
rs9271770 0.776 0.120 6 32626471 upstream gene variant G/A snv 0.76 10
rs9271695 0.776 0.080 6 32625303 upstream gene variant A/G snv 0.76 10
rs1028166
TENM3 ; TENM3-AS1
0.790 0.080 4 181892145 intron variant G/A snv 0.74 9
rs6031311
TOX2
0.776 0.080 20 44037835 intron variant C/T snv 0.73 10
rs3087967
C11orf53
0.776 0.080 11 111286111 3 prime UTR variant T/C snv 0.72 10
rs2179593
TOX2
0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs1391441
TET2-AS1 ; TET2
0.763 0.240 4 105207603 intron variant G/A snv 0.70 11
rs639933
C5orf66 ; LOC105379188
0.790 0.080 5 135132061 intron variant C/A snv 0.70 9
rs3787089
RTEL1-TNFRSF6B ; RTEL1
0.790 0.080 20 63685277 intron variant C/T snv 0.70 9
rs4143094
GATA3
0.752 0.240 10 8047173 intron variant T/G snv 0.70 12
rs847208 0.790 0.080 16 86220445 downstream gene variant C/A snv 0.70 9
rs6589219
COLCA2 ; COLCA1
0.790 0.080 11 111302186 intron variant G/C snv 0.69 9
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69 12
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17
rs3801081
TNS3
0.790 0.080 7 47471563 intron variant A/G snv 0.68 9
rs28488 0.776 0.080 20 6781574 downstream gene variant C/T snv 0.68 10