Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs4683946 0.925 0.080 3 101896982 intron variant G/T snv 0.19 2
rs115145466 1.000 0.080 6 32251264 upstream gene variant C/A;T snv 1
rs2621322 1.000 0.080 6 32820935 intron variant T/G snv 0.20 1
rs28780111 1.000 0.080 6 30752534 intron variant C/G;T snv 1
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 1
rs4112788 0.851 0.120 1 152578800 downstream gene variant A/G;T snv 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs115872194
BAG6
1.000 0.080 6 31639897 intron variant C/A;T snv 1
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 3
rs12044149
C1orf141
0.925 0.080 1 67135003 intron variant G/C;T snv 1
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 1
rs12356475
CTNNA3
1.000 0.080 10 66001962 intron variant T/C snv 0.15 1
rs149997688
DDR1
1.000 0.080 6 30893833 intron variant G/A snv 1
rs27044
ERAP1 ; LOC102724748
0.827 0.240 5 96783148 missense variant G/C snv 0.69 0.71 1
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 1
rs115645848
GABBR1
1.000 0.080 6 29622938 intron variant C/G;T snv 1
rs116199901
HCG18 ; HCG17
1.000 0.080 6 30315875 intron variant G/C snv 1
rs115112280
HCG23 ; TSBP1-AS1
1.000 0.080 6 32390772 non coding transcript exon variant T/A;G snv 1
rs115928623
HLA-A ; MICD
1.000 0.080 6 29971371 intron variant A/T snv 1
rs12191877
HLA-B
0.851 0.120 6 31285148 intron variant C/T snv 0.12 2
rs115429782
HLA-B ; LINC02571 ; LOC112267902
1.000 0.080 6 31297975 intron variant T/C snv 1
rs13191343
HLA-C ; HLA-B
1.000 0.080 6 31273332 intron variant C/G;T snv 0.13 1
rs9378127
HLA-DMA
1.000 0.080 6 32954682 intron variant G/A snv 0.11 1