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
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs514475 1.000 0.040 6 137717768 intron variant A/C snv 0.90 1
rs249038
ZFYVE16
1.000 0.040 5 80449650 missense variant A/G snv 0.91 0.87 1
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 6
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
rs7426056 0.807 0.120 2 203747335 regulatory region variant A/G snv 0.81 5
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 4
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs1008953 1.000 0.040 20 45352086 upstream gene variant T/C snv 0.79 1
rs140135
ZMAT5 ; UQCR10
0.827 0.120 22 29767846 non coding transcript exon variant C/G snv 0.79 5
rs36207871
CS
1.000 0.040 12 56290713 intron variant AGGAA/- delins 0.79 1
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
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 1
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
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
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
rs6548123
MYT1L
0.925 0.120 2 2221629 intron variant C/T snv 0.76 2
rs2451258
LOC112267968
0.807 0.160 6 159085568 intron variant C/T snv 0.75 6
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 2