Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555889984
RUNX1
0.925 0.120 21 34834536 stop gained C/A snv 5
rs267606640
AGL
0.882 0.120 1 99913557 stop gained G/A snv 5.6E-05 5.6E-05 5
rs9332377
ARVCF ; COMT
0.882 0.120 22 19968169 intron variant C/A;T snv 5
rs1057518925
COL6A2
1.000 0.120 21 46114006 splice acceptor variant A/G snv 4
rs11214105
TEX12 ; LOC107987164
1.000 0.120 11 112166930 intron variant G/A snv 0.25 2
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs4251961
IL1RN
0.763 0.200 2 113116890 intron variant T/C snv 0.29 10
rs4646437
CYP3A4
0.827 0.200 7 99767460 intron variant G/A snv 0.30 8
rs1331463984
TRAF7
0.701 0.240 16 2176350 missense variant G/A snv 33
rs1991517
LOC101928462 ; TSHR
0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 13
rs139194636
WARS2
0.882 0.240 1 119033203 missense variant T/C snv 6.4E-05 2.3E-04 6
rs757600616
WARS2
0.882 0.240 1 119033279 stop gained G/A snv 1.2E-05 6
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs151344517
LOC107985154 ; AFG3L2 ; TUBB6
0.742 0.320 18 12337505 missense variant C/T snv 31
rs864321670
ALDH18A1
0.763 0.320 10 95633012 missense variant C/T snv 24
rs181109321
TTPA
0.776 0.320 8 63065904 splice region variant C/A;T snv 2.0E-05 17
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49
rs869312697
ARID1B
0.882 0.400 6 157207241 stop gained C/T snv 8
rs1553621496
UNC80
0.677 0.440 2 209976305 splice donor variant T/G snv 53
rs121918459
PTPN11
0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 47
rs1554317002
LOC112267983 ; CDK13
0.724 0.440 7 39950821 frameshift variant C/- delins 45
rs224222
MEFV
0.724 0.440 16 3254463 missense variant C/T snv 0.24 0.21 15
rs1289543302
ABCB1
0.763 0.440 7 87536472 missense variant C/T snv 12