Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10750899 0.827 0.120 11 58517478 intergenic variant G/A snv 0.95 5
rs1049526
BRD2
0.925 0.040 6 32981027 3 prime UTR variant C/T snv 0.93 3
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 6
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 5
rs2249296
CLCA2
0.925 0.040 1 86444581 intron variant T/C snv 0.85 2
rs2328530
CDKAL1
0.827 0.120 6 20643496 intron variant G/A snv 0.85 5
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 1
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84 6
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 2
rs10801047 1.000 0.040 1 191590226 intergenic variant A/T snv 0.82 1
rs7426056 0.807 0.120 2 203747335 regulatory region variant A/G snv 0.81 5
rs2227564
PLAU ; C10orf55
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 3
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 4
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs11167764
LOC105378204
0.925 0.120 5 142099500 regulatory region variant A/C snv 0.80 1
rs140135
ZMAT5 ; UQCR10
0.827 0.120 22 29767846 non coding transcript exon variant C/G snv 0.79 5
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs6708413
IL18RAP
1.000 0.040 2 102446909 intron variant G/A snv 0.78 2
rs2058660
IL18RAP
0.882 0.280 2 102437989 intron variant G/A snv 0.78 1
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs6740462
LOC105374780
1.000 0.040 2 65440138 intron variant C/A snv 0.78 2
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 1
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 1
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 2