Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075800
HSPA1L
0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 8
rs703842
METTL1 ; CYP27B1
0.851 0.240 12 57768956 missense variant A/G snv 0.38 0.33 4
rs104895462
NOD2
0.882 0.120 16 50710911 missense variant C/T snv 3
rs1805110
TGFBR3
0.882 0.200 1 91861488 missense variant G/A snv 0.13 0.13 3
rs2287987
ERAP1
0.882 0.120 5 96793832 missense variant T/C snv 0.15 0.16 3
rs397514601
CAPN5
0.882 0.040 11 77115423 missense variant G/A;T snv 4.0E-06 3
rs104895460
NOD2
0.925 0.080 16 50711316 missense variant C/T snv 2
rs377679652
GRB10
0.925 0.040 7 50669861 missense variant C/T snv 4.6E-05 2.8E-05 2
rs1040461
RAB23
1.000 0.040 6 57190556 missense variant C/T snv 9.8E-02 0.12 1
rs1048709
CFB ; CYP21A2
0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs4752
GC
1.000 0.040 4 71756849 synonymous variant A/G snv 3.8E-02 8.6E-02 1
rs1128334
ETS1
0.851 0.160 11 128459064 3 prime UTR variant C/T snv 0.11 5
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs6841698 0.882 0.080 4 38760093 upstream gene variant G/A snv 0.36 4
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 6
rs10893872 0.882 0.120 11 128455658 downstream gene variant T/C snv 0.44 4