Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 9
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 8
rs177430
NPC1 ; RMC1
18 23506161 intron variant C/A;T snv 4
rs1056513
PATJ
1 61914626 missense variant G/A;C snv 0.57; 8.0E-06 3
rs12146733
FAIM2
12 49876581 intron variant G/C;T snv 3
rs1916799
FHIT
3 61247301 intron variant G/A;T snv 3
rs10018902 4 120941346 intergenic variant G/A;T snv 2
rs112540634
ILRUN
6 34656128 intron variant C/G;T snv 2
rs12625495
ZNF341
20 33775731 intron variant G/A;C;T snv 2
rs144582188 4 45163634 intergenic variant CTT/- delins 2
rs146144484 6 3865792 intron variant C/G;T snv 2
rs17668565 5 92818872 intergenic variant T/A;C snv 2
rs7777593 7 36506461 downstream gene variant T/A;G snv 2
rs11288989
NIPBL
5 37043527 intron variant AAA/-;A;AA;AAAA;AAAAA delins 1
rs1840440 18 25677222 intergenic variant T/C;G snv 1
rs286028
DLG2
11 85394069 intron variant A/C;T snv 1
rs3132479
LOC112267902 ; HLA-B
6 31306975 intron variant A/C;G snv 1
rs3785119
PRMT7
16 68340531 intron variant G/A;T snv 1
rs630372 1 177916627 intron variant G/A;T snv 1
rs6735049 2 630569 intergenic variant T/A;C snv 1
rs6780892 3 7947364 downstream gene variant G/A;T snv 1
rs759188048
MSRA
8 10066778 intron variant G/A;T snv 1
rs748156931
LINC02384
12 68434650 intron variant T/C snv 4.9E-05 1
rs761567588
CDYL
6 4790301 intron variant A/G snv 1.3E-04 2