Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11412402
EEFSEC
0.925 0.080 3 128194003 intron variant -/T ins 0.65 2
rs137939366
ELSPBP1
1.000 0.080 19 48019433 intron variant T/- del 1.5E-02 2
rs113092121
KIF11
0.925 0.080 10 92624756 intron variant -/CTCT delins 2
rs140522418
LOC107984408
0.925 0.080 11 128302942 intergenic variant A/-;AA delins 2
rs149317277
ITGB8
0.925 0.080 7 20384300 intron variant -/GAAACAAGATTCT;GAACCAAGATTCT delins 0.36 2
rs201541519 1.000 0.080 14 105694756 intergenic variant AAGA/- delins 1.2E-02 2
rs34445740
SMAD3
0.925 0.080 15 67183426 intron variant -/A delins 0.29 2
rs5875060
SCGN
1.000 0.080 6 25701740 3 prime UTR variant T/-;TT;TTT delins 2
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 7
rs16903574
OTULINL
0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 6
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 6
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 6
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs12365699 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 5
rs2066844
NOD2
0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 5