Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs296547
MROH3P
0.882 0.200 1 200923009 intron variant T/C snv 0.53 5
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs864537
CD247
0.925 0.200 1 167442147 intron variant A/G snv 0.29 4
rs2056626
CD247
0.882 0.080 1 167451188 intron variant T/G snv 0.30 3
rs3890745
MMEL1
0.925 0.200 1 2622185 intron variant T/C snv 0.40 3
rs4648356
TTC34
1.000 0.080 1 2792599 intron variant C/A snv 0.39 3
rs10752747
MMEL1
1 2593476 intron variant G/T snv 0.41 2
rs12138909
MMEL1
1 2607299 intron variant C/T snv 0.11 2
rs1772408
IFI16
1 159035859 intron variant A/G;T snv 2
rs7523907
LOC101928512 ; CD247
1.000 0.080 1 167458010 non coding transcript exon variant C/A;T snv 2
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs17035378
PLEK ; LOC101927723
0.882 0.200 2 68371823 intron variant T/A;C snv 5
rs4675374
ICOS ; LOC101927840
0.882 0.200 2 203937855 intron variant T/C snv 0.65 5
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs934734
SPRED2
0.925 0.160 2 65368452 intron variant G/A;T snv 0.54 4
rs13031237
REL
1.000 0.120 2 60908994 intron variant G/T snv 0.25 3
rs231804 0.925 0.200 2 203843923 intergenic variant C/T snv 0.60 3