Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13198610 1.000 0.120 6 32457895 downstream gene variant G/T snv 0.13 1
rs28895078 1.000 0.120 6 32450114 intergenic variant C/A;G snv 0.13 1
rs28895103 1.000 0.120 6 32451687 intergenic variant G/A snv 0.13 1
rs28895171 1.000 0.120 6 32455244 downstream gene variant G/A snv 0.13 1
rs28895187 1.000 0.120 6 32456603 downstream gene variant G/A snv 0.13 1
rs35571839 1.000 0.120 6 32544836 intergenic variant C/T snv 0.11 1
rs35998847 1.000 0.120 6 32699220 intergenic variant G/A snv 0.14 1
rs6054706 1.000 0.120 20 149223 downstream gene variant C/A;T snv 1
rs7755224 1.000 0.120 6 32684540 regulatory region variant A/G;T snv 1
rs587776633
BCL10
1.000 0.120 1 85270732 frameshift variant -/T delins 1
rs587776634
BCL10
1.000 0.120 1 85267788 frameshift variant TGCCTACTTCTAGAACA/- del 1
rs587776635
BCL10
1.000 0.120 1 85267919 frameshift variant T/- delins 1
rs587776636
BCL10
1.000 0.120 1 85267930 frameshift variant -/A delins 1
rs587776637
BCL10
1.000 0.120 1 85267692 inframe deletion TCT/- delins 1
rs372411058
FCGR3B
1.000 0.120 1 161626395 synonymous variant C/T snv 2.0E-05 4.2E-05 1
rs9274614
HLA-DQB1
1.000 0.120 6 32668069 intron variant C/A;G snv 1
rs28605404
HLA-DRB1
1.000 0.120 6 32601910 intergenic variant A/G snv 0.10 1
rs28530648
HLA-DRB6
1.000 0.120 6 32559302 intron variant A/C;T snv 1
rs1159838942
RAG1
1.000 0.120 11 36574757 missense variant C/A;T snv 1
rs2894253
TSBP1-AS1
1.000 0.120 6 32377763 intron variant T/G snv 1.0E-01 1
rs4760655
VDR
1.000 0.120 12 47900348 intron variant G/A snv 0.72 1
rs1493202
XKR9
1.000 0.120 8 70993352 intron variant T/G snv 0.41 1
rs17749561 0.925 0.120 18 63115978 intergenic variant G/A snv 5.9E-02 2
rs9275245 0.925 0.160 6 32693166 intergenic variant A/G;T snv 2
rs587776632
BCL10
0.925 0.120 1 85267901 frameshift variant A/-;AAA delins 2