Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs113191842
FTO
16 53783406 intron variant G/A snv 9.4E-02 5
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 5
rs177430
NPC1 ; RMC1
18 23506161 intron variant C/A;T snv 4
rs9813495
CADM2
3 85777231 intron variant A/G snv 0.15 4
rs1056513
PATJ
1 61914626 missense variant G/A;C snv 0.57; 8.0E-06 3
rs11863065 16 82293200 intergenic variant G/A snv 7.3E-02 3
rs12146733
FAIM2
12 49876581 intron variant G/C;T snv 3
rs1916799
FHIT
3 61247301 intron variant G/A;T snv 3
rs42377
CDK6
7 92614358 3 prime UTR variant G/A snv 0.28 3
rs7624084
ZBTB38
3 141374443 intron variant T/C snv 0.54 3
rs10018902 4 120941346 intergenic variant G/A;T snv 2
rs10198628 2 12824371 intron variant A/G snv 0.59 2
rs11030102
BDNF ; BDNF-AS
11 27660049 non coding transcript exon variant C/G snv 0.19 2
rs112540634
ILRUN
6 34656128 intron variant C/G;T snv 2
rs116975424
RFX3
9 3518833 intron variant T/C snv 2.6E-02 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
rs1650505 5 158602726 intergenic variant G/A snv 0.22 2
rs17668565 5 92818872 intergenic variant T/A;C snv 2
rs182381821 3 113643002 intergenic variant T/C snv 3.1E-03 2
rs28721484
PXYLP1 ; ZBTB38
3 141334437 intron variant C/T snv 0.22 2
rs397778224 16 19912366 regulatory region variant -/C delins 0.21 2
rs4477562 13 53530833 intron variant C/T snv 0.12 2