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
rs6911490
ATG5 ; PRDM1
1.000 0.040 6 106074152 intron variant T/C snv 0.86 1
rs2328530
CDKAL1
0.827 0.120 6 20643496 intron variant G/A snv 0.85 5
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84 6
rs943072 1.000 0.040 6 43828231 intron variant G/T snv 0.83 1
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 2
rs7426056 0.807 0.120 2 203747335 regulatory region variant A/G snv 0.81 5
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
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
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs6556411
LOC285626
0.827 0.120 5 159356215 intron variant G/T snv 0.77 5
rs941823
LINC00598
0.827 0.120 13 40439840 intron variant T/C snv 0.77 6
rs10743181 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 5
rs559928 0.827 0.120 11 64382898 intergenic variant T/C snv 0.77 6
rs7313895
LRRK2
0.827 0.120 12 40350592 intron variant G/T snv 0.77 5
rs3116494
CD28
0.882 0.120 2 203727298 intron variant G/A snv 0.76 2
rs3810936
TNFSF15
0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 1
rs2451258
LOC112267968
0.807 0.160 6 159085568 intron variant C/T snv 0.75 6
rs4263839
TNFSF15
0.807 0.160 9 114804160 intron variant A/G snv 0.75 1
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 2