Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
rs11757201 0.851 0.040 6 137682685 intron variant G/C;T snv 5
rs913678 0.882 0.240 20 50338887 regulatory region variant T/C snv 0.51 5
rs3757387
IRF5
0.851 0.280 7 128936032 upstream gene variant T/C snv 0.38 5
rs1800973
LYZ
0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 5
rs2066844
NOD2
0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 5
rs56177354
IRF8
1.000 0.040 16 85899046 upstream gene variant C/T snv 4.0E-02 3
rs2759663
CRB1
0.925 0.080 1 197415296 intron variant C/G;T snv 2
rs62491812
GIMAP6
1.000 0.040 7 150630336 intron variant C/A snv 0.18 2
rs4313034
HLA-J ; ZNRD1ASP ; HLA-A
0.925 0.160 6 30006148 non coding transcript exon variant C/T snv 0.78 2
rs1353248
IL12A-AS1
0.925 0.120 3 159905770 intron variant C/T snv 0.32 2
rs668998
IL12A-AS1
0.925 0.120 3 159997764 non coding transcript exon variant G/A snv 0.63 2
rs76830965
IL12A-AS1
0.925 0.120 3 159919889 intron variant C/A;G;T snv 2
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs4921484
LOC285626
1.000 0.040 5 159342745 intron variant T/C snv 0.78 2
rs2517664
TRIM31-AS1 ; TRIM31
1.000 0.040 6 30105482 non coding transcript exon variant C/T snv 0.21 2
rs10411970 1.000 0.040 19 4814636 downstream gene variant C/A;G snv 1
rs10817678 1.000 0.040 9 114817177 intergenic variant G/A snv 0.74 1
rs11649485 1.000 0.040 16 85980849 intron variant A/G snv 0.18 1
rs11989430 1.000 0.040 8 89806387 regulatory region variant A/T snv 0.22 1
rs150383292 1.000 0.040 3 161562034 intergenic variant C/T snv 1.0E-02 1
rs17552787 1.000 0.040 7 50264486 upstream gene variant C/A;T snv 1
rs2429657 1.000 0.040 6 30503743 intergenic variant A/G snv 0.21 1
rs2523589 0.851 0.200 6 31359557 upstream gene variant G/A;T snv 1
rs3135461 1.000 0.040 6 32712345 regulatory region variant G/A;C snv 1