Source: CURATED ×
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 39
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 6
rs56167332 0.807 0.160 5 159400761 intron variant C/A;T snv 6
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 5
rs6871626 0.851 0.160 5 159399784 intron variant C/A;G snv 0.29 3
rs8111
ATF6B ; TNXB
0.925 0.160 6 32115398 3 prime UTR variant C/T snv 0.26 3
rs10919543 1.000 0.080 1 161538827 intron variant A/G snv 0.28 2
rs12524487 0.925 0.160 6 31386461 upstream gene variant C/T snv 5.9E-02 2
rs2099684 1.000 0.080 1 161530340 intron variant A/G snv 0.28 2
rs4817984 1.000 0.080 21 39093140 intergenic variant C/A;G snv 2
rs1383258
HLA-DOB
0.925 0.160 6 32815628 intron variant C/T snv 8.3E-02 2
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 2
rs10921544 1.000 0.080 1 194360431 intergenic variant C/G;T snv 1
rs12321966 1.000 0.080 12 8548569 non coding transcript exon variant G/T snv 9.4E-02 1
rs12608210 1.000 0.080 18 24913920 intron variant G/A snv 0.31 1
rs17133698 1.000 0.080 6 255562 regulatory region variant C/T snv 6.5E-02 1
rs3869115 1.000 0.080 6 31236917 intergenic variant C/G snv 9.5E-02 1
rs4463283 1.000 0.080 6 29097215 upstream gene variant C/A;T snv 8.1E-02 1
rs4817988 1.000 0.080 21 39096912 regulatory region variant G/A snv 0.26 1
rs4921492 0.925 0.120 5 159405269 intron variant C/A;G snv 1
rs4921493 0.925 0.080 5 159409099 intron variant T/A;C snv 1
rs7603494 1.000 0.080 2 47676957 intergenic variant C/T snv 0.57 1
rs7843437 1.000 0.080 8 69925162 upstream gene variant C/A snv 0.30 1
rs9266745 1.000 0.080 6 31383435 upstream gene variant G/A snv 0.71 1
rs9271539 1.000 0.080 6 32622251 regulatory region variant G/A snv 0.36 1