Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs708567
IL17RC
0.807 0.200 3 9918386 missense variant C/T snv 0.46 0.51 6
rs1050829
G6PD
0.827 0.160 X 154535277 missense variant T/A;C snv 1.7E-04; 2.6E-02 5
rs1057520529
FOXP3
0.851 0.320 X 49251440 missense variant C/T snv 5
rs121918367
SLC11A2
0.827 0.080 12 50999214 missense variant C/A;T snv 6.0E-05 5
rs13194491 1.000 0.040 6 27069301 intergenic variant C/T snv 4.8E-02 5
rs776035233
LCAT
0.882 0.120 16 67940230 missense variant C/T snv 4.0E-06 5
rs878853314
GBA
0.882 0.240 1 155239655 missense variant C/G snv 5
rs878853315
GBA
0.925 0.160 1 155236292 missense variant G/C snv 5
rs104894808
GATA1
0.851 0.120 X 48792376 missense variant G/T snv 4
rs1060499688
GNPTAB
0.882 0.200 12 101753399 missense variant A/G snv 4
rs1934951
CYP2C8
0.925 0.160 10 95038791 intron variant C/T snv 0.24 4
rs747506979
GBA
0.882 0.160 1 155235003 missense variant G/A snv 1.2E-05 4
rs779114194
LCAT
0.925 0.120 16 67940017 missense variant T/C snv 1.4E-05 4
rs987710
IGLV10-54
1.000 0.040 22 22158022 intron variant G/A snv 0.61 4
rs10132552
MEG3
1.000 0.040 14 100834675 non coding transcript exon variant T/C snv 0.25 3
rs10761745
JMJD1C
0.882 0.240 10 63341311 intron variant G/C snv 0.87 3
rs2071346
MYC ; CASC11
0.925 0.160 8 127736777 intron variant G/T snv 7.1E-02 3
rs41469945
HBA2
0.925 0.080 16 173581 missense variant T/C;G snv 3
rs4150558
GTF2H1
0.882 0.040 11 18332808 non coding transcript exon variant T/A snv 8.7E-03 3
rs41518645
ND6 ; CYTB
0.925 0.200 MT 15257 missense variant G/A snv 3
rs4645948
MYC ; CASC11
0.882 0.160 8 127736252 synonymous variant C/T snv 2.8E-02 3
rs6051702
C20orf194
0.882 0.120 20 3271278 intron variant A/C snv 0.19 3
rs760370
SLC29A1
0.925 0.120 6 44233216 intron variant A/G snv 0.36 3
rs775910328
TLR4
0.882 0.120 9 117713471 missense variant A/G snv 4.0E-06 3
rs866082104
ABCB7
0.925 0.120 X 75053456 missense variant C/T snv 3