Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1876453
CR2
0.851 0.160 1 207454573 intron variant G/A snv 8.4E-02 4
rs1048971
CR2
0.851 0.160 1 207472977 synonymous variant G/A;T snv 0.34; 8.0E-06 4
rs17615
CR2
0.827 0.200 1 207473117 missense variant G/A snv 0.26 0.31 5
rs1341239
PRL ; CASC15
0.776 0.360 6 22303975 intron variant A/C snv 0.65 8
rs1206255976
C1QA
0.851 0.160 1 22637618 start lost T/G snv 7.0E-06 4
rs292001
C1QA
0.807 0.320 1 22638465 intron variant G/A snv 0.54 6
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs3131379
MSH5 ; MSH5-SAPCD1
0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 10
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 11
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs121908117
ATRIP ; TREX1 ; ATRIP-TREX1
0.708 0.440 3 48466707 missense variant G/A snv 17
rs72556554
ATRIP ; TREX1 ; ATRIP-TREX1
0.776 0.400 3 48466996 missense variant G/A;C snv 2.1E-04; 2.7E-04 9
rs370504038
ATRIP-TREX1 ; ATRIP ; SHISA5 ; TREX1
0.851 0.160 3 48467569 missense variant A/G snv 1.2E-04 1.2E-04 4
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs2397084
IL17F
0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs1678542
KIF5A
0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25