Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72699866
RIN3
14 92648442 intron variant G/A snv 0.14 4
rs884205
TNFRSF11A
18 62387624 3 prime UTR variant A/C;T snv 4
rs2908004
WNT16
1.000 0.040 7 121329715 missense variant G/A;T snv 0.44; 4.0E-06 4
rs10048146 1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17 3
rs1564981 16 50952397 intergenic variant G/A snv 0.60 3
rs4580892 6 127088737 intron variant C/T snv 0.32 3
rs6426749 1.000 0.080 1 22384980 intergenic variant G/C snv 0.19 3
rs6532023 1.000 0.080 4 87852697 regulatory region variant T/G snv 0.66 3
rs6913578 0.925 0.080 6 151628671 intergenic variant A/C;T snv 3
rs9525638 13 42554441 regulatory region variant T/C snv 0.37 3
rs4870044
CCDC170
1.000 0.080 6 151580274 intron variant C/T snv 0.44 3
rs13245690
CPED1
7 121145010 intron variant A/G snv 0.32 3
rs917727
FAM3C
7 121378525 intron variant C/A;T snv 0.33 3
rs7466269
FUBP3
9 130588697 intron variant A/G snv 0.33 3
rs1054627
IBSP
1.000 0.080 4 87811540 missense variant G/A snv 0.30 0.24 3
rs2273061
JAG1
1.000 0.080 20 10658895 intron variant G/A snv 0.46 3
rs9533090
LINC02341
13 42377313 intron variant C/T snv 0.39 3
rs1107748
LINC02594
1.000 0.080 17 43696446 intron variant T/C snv 0.54 3
rs10085588
LOC105375412 ; SEM1 ; LOC105375411
1.000 0.080 7 96508362 intron variant A/G snv 0.72 3
rs56318008
LOC105376845 ; WNT4
0.925 0.120 1 22143914 5 prime UTR variant C/T snv 0.13 3
rs10037512
MEF2C-AS1
5 89058858 intron variant T/A;C snv 3
rs1366594
MEF2C-AS1
5 89080244 intron variant A/C snv 0.57 3
rs6894139
MEF2C-AS1
5 89031965 non coding transcript exon variant T/G snv 0.57 3
rs1595824
PLCL1
2 198009282 intron variant C/A;T snv 3
rs12283755
PPP6R3
11 68604190 intron variant A/G snv 0.24 3