Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 15
rs1859168
HOTTIP
0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 13
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 7
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 7
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs2067087
HOTTIP ; HOXA13
1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 6
rs419076
MECOM
3 169383098 intron variant T/A;C snv 6
rs9292468 5 32818967 intergenic variant T/A;C snv 6
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs10184428 2 164155317 intron variant C/A;G snv 5
rs12258967
CACNB2
10 18439030 intron variant C/G;T snv 5
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5