Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs2178146 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 8
rs398122820
B2M
0.790 0.240 15 44715641 missense variant G/A snv 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
rs12035735
LRRC8D
1 89839786 intron variant G/A snv 1.4E-03 4
rs121908377
FOXP2
1.000 0.120 7 114662075 missense variant G/A snv 3