Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs180177035
BRAF
0.752 0.280 7 140801502 missense variant T/C snv 35
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs238406
ERCC2
0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs121908120
WNT10A
0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 19
rs9282858
SRD5A2
0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 16
rs116855232
NUDT15
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 12
rs2740574
CYP3A4
0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78 12
rs2294020
CCDC22
0.763 0.280 X 49246763 missense variant A/G;T snv 10
rs5934505 0.776 0.120 X 8945785 intergenic variant T/A;C snv 10
rs12373124
SPPL2C ; MAPT-AS1
0.790 0.120 17 45846853 synonymous variant T/C snv 0.15 0.14 9
rs6152
AR
0.763 0.240 X 67545785 synonymous variant G/A snv 0.15 0.28 9
rs201249971
LIPH
0.776 0.120 3 185519292 missense variant A/T snv 1.6E-04 4.9E-05 8
rs10502861
SLC14A2
0.807 0.080 18 45220183 intron variant C/T snv 0.32 7
rs10888690
FAF1
0.807 0.080 1 50494849 intron variant T/A;C snv 7
rs10930758 0.807 0.080 2 176897100 intergenic variant A/G;T snv 7
rs11037975 0.807 0.080 11 44389312 intergenic variant C/A;G snv 7
rs115182912 0.807 0.080 3 126274431 intron variant G/A snv 1.5E-02 7
rs11593840
LRMDA
0.807 0.080 10 76436854 intron variant A/G snv 0.40 7