Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800972
DEFB1
0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
rs11362
DEFB1
0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 13
rs1799946
DEFB1
0.732 0.360 8 6877909 5 prime UTR variant C/T snv 0.36 0.41 13
rs7229639
SMAD7
0.763 0.080 18 48924606 intron variant A/G snv 0.87 13
rs2178146 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 8
rs2687201 0.925 0.080 3 70879779 intergenic variant A/C;G snv 6
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv 6
rs11789015
BARX1
0.882 0.080 9 93953746 intron variant A/C;G snv 6
rs4800353 0.925 0.080 18 22074176 intergenic variant A/G snv 0.30 5
rs10419226
CRTC1
0.925 0.080 19 18692362 intron variant T/G snv 0.67 5
rs7632500
LOC107986152
0.925 0.080 3 168007561 downstream gene variant A/G snv 0.17 5
rs7240004 1.000 0.040 18 48868651 intergenic variant A/G snv 0.43 4
rs12035735
LRRC8D
1 89839786 intron variant G/A snv 1.4E-03 4