Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2280141
PLEKHA1
1.000 0.040 10 122433665 3 prime UTR variant T/G snv 0.56 3
rs6585827
PLEKHA1
1.000 0.040 10 122406099 intron variant G/A snv 0.47 3
rs6848139 1.000 0.040 4 122473886 intergenic variant A/C;G snv 2
rs2108225 1.000 0.040 7 107812658 downstream gene variant G/A;T snv 1
rs2456973
LOC105369781 ; IKZF4 ; LOC105369780
0.925 0.040 12 56023144 intron variant A/C;G snv 1
rs7088058
PLEKHA1
0.851 0.040 10 122389836 intron variant C/T snv 0.32 1
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 3
rs2056626
CD247
0.882 0.080 1 167451188 intron variant T/G snv 0.30 3
rs212402
LOC105378083
1.000 0.080 6 159051263 intron variant G/A snv 0.66 3
rs2249937
LOC112267968
1.000 0.080 6 159094277 non coding transcript exon variant T/G snv 0.76 3
rs4648356
TTC34
1.000 0.080 1 2792599 intron variant C/A snv 0.39 3
rs654690
LOC112267968
1.000 0.080 6 159093746 intron variant T/A;C snv 3
rs657555
PTPN2
0.925 0.080 18 12847137 intron variant C/A;T snv 3
rs715412 1.000 0.080 11 118813901 regulatory region variant G/A snv 0.17 3
rs6726160
NONOP2
1.000 0.080 2 60937594 non coding transcript exon variant T/G snv 0.47 2
rs7523907
LOC101928512 ; CD247
1.000 0.080 1 167458010 non coding transcript exon variant C/A;T snv 2
rs11711054 1.000 0.080 3 46304120 intergenic variant G/A snv 0.73 1
rs17066096 1.000 0.080 6 137131771 intergenic variant A/G snv 0.20 1
rs638893 0.882 0.080 11 118827828 intergenic variant G/A snv 0.79 1
rs5754217
UBE2L3
0.925 0.120 22 21585386 intron variant G/T snv 0.31 5
rs10892258
LOC105369519
0.925 0.120 11 118709156 intron variant G/A snv 0.19 4
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs13031237
REL
1.000 0.120 2 60908994 intron variant G/T snv 0.25 3
rs1953126
PHF19
1.000 0.120 9 120878222 intron variant T/C snv 0.68 3
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 2