Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397514601
CAPN5
0.882 0.040 11 77115423 missense variant G/A;T snv 4.0E-06 3
rs377679652
GRB10
0.925 0.040 7 50669861 missense variant C/T snv 4.6E-05 2.8E-05 2
rs10044354
LNPEP
1.000 0.040 5 96984791 intron variant C/T snv 0.41 1
rs1040461
RAB23
1.000 0.040 6 57190556 missense variant C/T snv 9.8E-02 0.12 1
rs2358820
VTCN1
1.000 0.040 1 117169289 intron variant G/A snv 5.3E-02 1
rs4752
GC
1.000 0.040 4 71756849 synonymous variant A/G snv 3.8E-02 8.6E-02 1
rs7519847
CELA3A
1.000 0.040 1 22003194 intron variant C/G;T snv 1
rs6841698 0.882 0.080 4 38760093 upstream gene variant G/A snv 0.36 4
rs104895460
NOD2
0.925 0.080 16 50711316 missense variant C/T snv 2
rs61860052
ANXA11
0.925 0.080 10 80201955 intron variant C/A snv 6.4E-02 2
rs10893872 0.882 0.120 11 128455658 downstream gene variant T/C snv 0.44 4
rs104895462
NOD2
0.882 0.120 16 50710911 missense variant C/T snv 3
rs2287987
ERAP1
0.882 0.120 5 96793832 missense variant T/C snv 0.15 0.16 3
rs6703630
IL19
0.925 0.120 1 206775294 intron variant C/T snv 0.25 2
rs1128334
ETS1
0.851 0.160 11 128459064 3 prime UTR variant C/T snv 0.11 5
rs2222202
IL10 ; IL19
0.827 0.160 1 206772036 intron variant G/A snv 0.39 5
rs12722489
IL2RA
0.882 0.160 10 6060049 intron variant C/T snv 0.11 3
rs7565639
PDCD1 ; LOC105373977
0.882 0.160 2 241854911 intron variant T/A;C snv 3
rs7421861
LOC105373977 ; PDCD1
0.790 0.200 2 241853198 intron variant A/G;T snv 9
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 6
rs1805110
TGFBR3
0.882 0.200 1 91861488 missense variant G/A snv 0.13 0.13 3
rs6710479
LOC105373977 ; PDCD1
0.882 0.200 2 241855866 intron variant T/C snv 0.51 3
rs2489188
TGFBR3
0.925 0.200 1 91866932 intron variant C/T snv 0.65 2
rs703842
METTL1 ; CYP27B1
0.851 0.240 12 57768956 missense variant A/G snv 0.38 0.33 4
rs10863888
TRAF5
0.851 0.280 1 211329427 intron variant A/C;G;T snv 4