Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1682093 2 22551319 downstream gene variant C/T snv 0.95 1
rs6711710
KCNE4
2 223091692 intron variant T/C snv 0.77 2
rs3818416
EDNRB-AS1 ; EDNRB
1.000 0.080 13 77900333 intron variant A/C snv 0.75 3
rs1884429 1 11052779 downstream gene variant T/C snv 0.74 2
rs8082345 17 48949756 upstream gene variant C/A snv 0.73 1
rs7740188
L3MBTL3
6 130024960 intron variant G/A snv 0.73 1
rs2885697
SCMH1
1.000 0.080 1 41078607 intron variant G/T snv 0.72 2
rs10068807 5 55581157 intergenic variant A/G snv 0.70 1
rs5750823
TAB1 ; LOC100506472
22 39433968 intron variant C/T snv 0.70 3
rs183041 5 177099269 downstream gene variant G/A snv 0.70 1
rs508347
JAZF1
7 28173205 intron variant T/C snv 0.69 2
rs212526
ECE1
1 21258448 intron variant T/C snv 0.68 2
rs6544334
SLC8A1
2 40369384 intron variant A/C snv 0.68 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs11874191 18 38584120 intergenic variant C/T snv 0.66 1
rs10917220 1 22356912 intergenic variant T/C snv 0.65 1
rs2943656 1.000 0.080 2 226257202 regulatory region variant A/G snv 0.63 2
rs7048601
TEX10
9 100311981 intron variant G/T snv 0.63 1
rs12509014
NUDT6
4 122904764 intron variant C/T snv 0.63 2
rs4842924
ADAMTSL3
15 83918855 intron variant C/T snv 0.63 1
rs1991083
KLHL29
2 23664567 intron variant C/T snv 0.62 1
rs1884762
KIZ
20 21144026 intron variant G/C snv 0.62 1
rs7310698
PDE3A
12 20413457 intron variant G/A;C snv 0.61 1
rs4819021 21 45047012 intergenic variant T/C snv 0.59 1
rs1228024 11 47929801 regulatory region variant C/A snv 0.56 1