Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1391441
TET2-AS1 ; TET2
0.763 0.240 4 105207603 intron variant G/A snv 0.70 11
rs4562
ELP5 ; CLDN7
0.925 0.080 17 7260420 missense variant A/G snv 0.65 0.70 3
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
rs6588147
LEPR
0.851 0.080 1 65469811 intron variant G/A snv 0.70 4
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
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
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
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 16
rs6598964
LIN28A
0.882 0.080 1 26419836 intron variant A/G snv 0.67 3
rs10049390
SLCO2A1
0.776 0.080 3 133982275 intron variant G/A snv 0.67 10
rs7542665
L1TD1
0.790 0.080 1 62207365 missense variant T/C snv 0.63 0.67 9
rs16944613
LOC112268163 ; CRTC3
0.790 0.080 15 90595866 non coding transcript exon variant A/G snv 0.67 9
rs812481
LRIG1
0.790 0.080 3 66392011 intron variant C/G snv 0.66 9
rs1741640
LAMA5
0.776 0.080 20 62357358 intron variant T/C snv 0.66 10
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs61336918 0.790 0.080 16 79973369 intergenic variant A/T snv 0.65 9
rs1886450 0.790 0.080 13 73412491 upstream gene variant A/G snv 0.65 9