Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs140751051
MNX1
1.000 0.080 7 157000756 intron variant -/A delins 1
rs11410487
PELO ; ITGA1
1.000 0.080 5 52798410 intron variant -/T delins 0.91 1
rs144226500
FAAH2
1.000 0.080 X 57144348 intergenic variant -/T;TT delins 1
rs68062313
ATP8B2
1.000 0.080 1 154337120 intron variant A/- del 0.69 1
rs11390176
IL13RA1
1.000 0.080 X 118781201 intron variant A/-;AA;AAA delins 1
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 4
rs10974438
GLIS3
0.925 0.120 9 4291928 intron variant A/C snv 0.29 3
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 2
rs115689251
LOC107985068
1.000 0.080 17 36032377 intergenic variant A/C snv 1.0E-02 2
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 2
rs11873305 1.000 0.080 18 60381959 intron variant A/C snv 0.12 2
rs75298135 1.000 0.080 5 28184372 intergenic variant A/C snv 1.3E-02 2
rs7929543 0.925 0.120 11 49329474 intron variant A/C snv 0.12 2
rs9472719 1.000 0.080 6 46183649 regulatory region variant A/C snv 0.32 2
rs9896052 0.882 0.160 17 75422781 intergenic variant A/C snv 0.50 2
rs9942471 0.925 0.160 6 89238513 intergenic variant A/C snv 0.37 2
rs10100265
PINX1
1.000 0.080 8 10775649 intron variant A/C snv 0.60 1
rs10517030
PPARGC1A
0.925 0.120 4 23961283 intergenic variant A/C snv 6.9E-02 1
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 1
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 1
rs12500426
PDLIM5
0.851 0.240 4 94593458 intron variant A/C snv 0.54 1
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 1
rs202178099 1.000 0.080 5 50927276 downstream gene variant A/C snv 3.2E-02 1
rs2283228
KCNQ1
1.000 0.080 11 2828300 intron variant A/C snv 0.10 1
rs2943640 1.000 0.080 2 226228869 intergenic variant A/C snv 0.75 1