Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 7
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 7
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs11953630 5 158418394 intergenic variant C/A;T snv 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs35444 12 115114632 intergenic variant A/G snv 0.38 6
rs419076
MECOM
3 169383098 intron variant T/A;C snv 6
rs62434129
PLEKHG1
6 150687701 intron variant A/G;T snv 8.8E-02 6
rs8068318
TBX2
17 61406405 non coding transcript exon variant C/T snv 0.56 6
rs9292468 5 32818967 intergenic variant T/A;C snv 6