Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34436714
NLRP12
0.851 0.120 19 53824059 missense variant C/A;T snv 0.22 7
rs4358188
BPI
0.827 0.160 20 38318446 missense variant G/A;C snv 0.46 7
rs56167332 0.807 0.160 5 159400761 intron variant C/A;T snv 7
rs5743293
NOD2
0.807 0.200 16 50729868 frameshift variant C/-;CC delins 7
rs6596473
SLC23A1
0.807 0.120 5 139374887 intron variant G/C;T snv 7
rs7556897 0.807 0.120 2 227795396 intergenic variant C/G;T snv 7
rs1384936174
NOD2
0.827 0.040 16 50710812 missense variant G/A;T snv 4.0E-06; 4.0E-06 6
rs1545620
MYO9B
0.827 0.080 19 17192965 missense variant T/A;G snv 1.3E-05; 0.52 6
rs259964
ZNF831
0.827 0.120 20 59249254 intron variant A/G;T snv 6
rs387906536
LYZ
0.851 0.200 12 69350215 missense variant T/A;C snv 6
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 6
rs4946717
PRDM1
0.827 0.120 6 106026874 intron variant C/A;G;T snv 6
rs57749775
KRT8
0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 6
rs7097656
TSPAN14
0.827 0.120 10 80491075 intron variant T/C;G snv 6
rs71559680 0.827 0.120 6 21430497 intergenic variant TAG/CAT mnv 6
rs774229224
PLG
0.882 0.160 6 160706454 missense variant C/A;G snv 4.0E-06; 4.0E-06 6
rs1020856343
SLC22A5
0.851 0.240 5 132393705 missense variant C/T snv 4.0E-06 5
rs104895094
MEFV
0.851 0.320 16 3243403 missense variant T/A;C snv 8.0E-06; 5.2E-03 5
rs10951982
RAC1
0.851 0.160 7 6382925 intron variant G/A;T snv 5
rs2160322
MAGI2
0.851 0.160 7 78462650 intron variant G/A;C snv 5
rs2274907
ITLN1
0.851 0.200 1 160882036 missense variant A/G;T snv 0.66 5
rs3731865
SLC11A1
0.882 0.160 2 218385280 non coding transcript exon variant G/A;C;T snv 0.23; 1.4E-04 5
rs6074022 0.851 0.240 20 46111557 TF binding site variant C/G;T snv 5
rs758548184
NOD2
0.851 0.240 16 50699557 missense variant G/C snv 5
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 5