Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34445740
SMAD3
0.925 0.080 15 67183426 intron variant -/A delins 0.29 2
rs113092121
KIF11
0.925 0.080 10 92624756 intron variant -/CTCT delins 2
rs149317277
ITGB8
0.925 0.080 7 20384300 intron variant -/GAAACAAGATTCT;GAACCAAGATTCT delins 0.36 2
rs11412402
EEFSEC
0.925 0.080 3 128194003 intron variant -/T ins 0.65 2
rs140522418
LOC107984408
0.925 0.080 11 128302942 intergenic variant A/-;AA delins 2
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs2051809
KIF3A
1.000 0.080 5 132721182 intron variant A/C snv 0.58 1
rs35141484
LOC105374418 ; KLHL5
1.000 0.080 4 39086721 synonymous variant A/C snv 5.6E-03 2.2E-02 1
rs12531500 0.925 0.080 7 20504586 intergenic variant A/C;G snv 2
rs17103286 0.925 0.080 14 35415835 regulatory region variant A/C;G snv 2
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs2378383 1.000 0.080 9 79424447 intergenic variant A/C;G;T snv 1
rs2299012
RAD50
0.925 0.080 5 132581248 intron variant A/C;T snv 2
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 5
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 4
rs17144046 0.882 0.120 10 8564051 intergenic variant A/G snv 0.28 4
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 4
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs9391997
IRF4
0.851 0.160 6 409119 3 prime UTR variant A/G snv 0.38 4
rs13277355 0.882 0.120 8 127765473 intergenic variant A/G snv 0.71 3
rs449454
NDFIP1
0.925 0.080 5 142153497 3 prime UTR variant A/G snv 0.65 0.68 3
rs7518129
TNFSF4
0.882 0.120 1 173194429 intron variant A/G snv 0.47 3