Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1568952 1.000 0.080 8 58799804 intergenic variant T/C snv 0.75 1
rs6507226 1.000 0.080 18 22611328 intergenic variant A/G snv 0.45 1
rs9271300 1.000 0.080 6 32613805 intergenic variant C/G snv 0.54 1
rs3092923
CD40LG
1.000 0.080 X 136659026 intron variant T/C snv 0.17 0.28 1
rs10841847
CLEC4E
1.000 0.080 12 8535216 intron variant A/G snv 0.58 1
rs15493
GPHN ; VTI1B ; ARG2
1.000 0.080 14 67651415 missense variant C/G;T snv 9.2E-02 8.8E-02 1
rs9272461
HLA-DQA2 ; HLA-DQA1 ; LOC107986589
1.000 0.080 6 32637832 intron variant G/A snv 0.13 1
rs2230424
ITGAX
1.000 0.080 16 31355997 missense variant T/C snv 8.6E-02 9.0E-02 1
rs2660898
LTA4H
1.000 0.080 12 96032219 intron variant T/G snv 0.30 1
rs1371562
MARCO
1.000 0.080 2 118975372 intron variant G/T snv 0.33 1
rs17009726
MARCO
1.000 0.080 2 118967884 intron variant A/G snv 1.0E-02 1
rs17795618
MARCO
1.000 0.080 2 118973892 intron variant T/A snv 0.12 1
rs2011839
MARCO
1.000 0.080 2 118985008 intron variant C/A;T snv 1
rs2278589
MARCO
1.000 0.080 2 118971300 intron variant G/A;C snv 1
rs6761637
MARCO
1.000 0.080 2 118981487 missense variant T/C snv 8.3E-02 0.13 1
rs3774275
MASP1
1.000 0.080 3 187247480 intron variant A/G snv 0.22 1
rs11575886
MC3R
1.000 0.080 20 56248494 upstream gene variant A/G snv 8.0E-02 1
rs9905742
MYBBP1A
1.000 0.080 17 4539780 missense variant T/A snv 3.0E-02 2.7E-02 1
rs1050504
NSMAF
1.000 0.080 8 58583857 3 prime UTR variant C/T snv 0.24 1
rs208290
P2RX7 ; LOC105370032
1.000 0.080 12 121156253 intron variant G/A snv 0.43 1
rs656612
P2RX7 ; LOC105370032
1.000 0.080 12 121138849 intron variant C/A snv 0.60 1
rs1057141
PSMB9 ; TAP1
1.000 0.080 6 32850997 missense variant T/C snv 0.20 0.20 1
rs3859664
SIGLEC1
1.000 0.080 20 3691244 intron variant G/A snv 0.34 1
rs10208770
SP110
1.000 0.080 2 230170151 intron variant T/G snv 0.14 1
rs10498244
SP110
1.000 0.080 2 230173117 non coding transcript exon variant T/C snv 0.26 1