Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174621
FADS2
1.000 11 61862632 non coding transcript exon variant G/A;C snv 2
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 4
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 8
rs11178648
TSPAN8
0.925 0.080 12 71139430 intron variant C/T snv 0.29 2
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5
rs4739738 0.882 0.120 8 80379410 intron variant G/A snv 0.60 3
rs35204956 0.925 0.080 8 80389778 intron variant A/-;AA;AAA delins 2
rs11255504
GATA3
0.925 0.080 10 8062378 intron variant A/G;T snv 2
rs7099257 0.925 0.080 10 8468994 upstream gene variant T/A snv 0.49 2
rs10795672 0.925 0.080 10 8735677 intergenic variant G/A;T snv 2
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3
rs58521088
BACH2
0.925 0.080 6 90275479 intron variant A/T snv 0.27 2
rs1321859
LOC105377891
0.925 0.080 6 90301954 intron variant C/T snv 0.24 2
rs4771332 0.925 0.080 13 99418203 upstream gene variant T/A;C;G snv 2