Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 7
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs35998847 1.000 0.120 6 32699220 intergenic variant G/A snv 0.14 1
rs9275517
MTCO3P1
0.925 0.200 6 32706872 non coding transcript exon variant A/G snv 0.58 2
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs2621416 0.882 0.280 6 32774091 intergenic variant T/C snv 0.26 4
rs3117222
HLA-DPA2
0.882 0.280 6 33093172 intron variant C/T snv 0.33 3
rs2855429
COL11A2
0.925 0.120 6 33190412 intron variant A/C snv 0.78 2
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs1494555
IL7R
0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs1159838942
RAG1
1.000 0.120 11 36574757 missense variant C/A;T snv 1
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs3212961
ERCC1
0.827 0.200 19 45419065 intron variant G/A;T snv 1.9E-04; 0.20 7
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs4760655
VDR
1.000 0.120 12 47900348 intron variant G/A snv 0.72 1
rs17749561 0.925 0.120 18 63115978 intergenic variant G/A snv 5.9E-02 2
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1493202
XKR9
1.000 0.120 8 70993352 intron variant T/G snv 0.41 1
rs764562217
TP53
0.882 0.120 17 7673308 stop lost T/G snv 2.3E-05 3.5E-05 3
rs587781386
TP53
0.882 0.120 17 7674889 missense variant A/C;G snv 3.2E-05; 4.0E-06 3
rs8094402
MBP
0.882 0.120 18 76995493 intron variant A/G snv 0.25 3
rs2682818
MIR618 ; LOC105369869 ; LIN7A
0.742 0.320 12 80935757 non coding transcript exon variant A/C;T snv 0.83 14
rs1805377
XRCC4
0.689 0.480 5 83353124 splice acceptor variant G/A snv 0.23 0.25 19
rs1056503
XRCC4
0.851 0.200 5 83353158 synonymous variant T/A;G snv 4.0E-06; 0.23 4