Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
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
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs72556554
ATRIP ; TREX1 ; ATRIP-TREX1
0.776 0.400 3 48466996 missense variant G/A;C snv 2.1E-04; 2.7E-04 9
rs1518110
IL10 ; IL19
0.851 0.160 1 206771516 intron variant A/C;T snv 5
rs1048971
CR2
0.851 0.160 1 207472977 synonymous variant G/A;T snv 0.34; 8.0E-06 4
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1206255976
C1QA
0.851 0.160 1 22637618 start lost T/G snv 7.0E-06 4
rs370504038
ATRIP-TREX1 ; ATRIP ; SHISA5 ; TREX1
0.851 0.160 3 48467569 missense variant A/G snv 1.2E-04 1.2E-04 4
rs3093061
CRP
0.851 0.160 1 159715192 upstream gene variant T/C snv 4.8E-02 4
rs2397084
IL17F
0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 11
rs3131379
MSH5 ; MSH5-SAPCD1
0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 10
rs1876453
CR2
0.851 0.160 1 207454573 intron variant G/A snv 8.4E-02 4
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs2070197
IRF5
0.827 0.280 7 128948946 3 prime UTR variant T/C snv 9.0E-02 6
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs3813946
CR2
0.827 0.280 1 207454348 5 prime UTR variant T/C snv 0.16 5
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs1050501
FCGR2B
0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15