Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 64
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 38
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 36
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 28
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 22
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 18
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 16
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 14
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 13
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 13
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 12
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 12
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 12
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 12
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 12
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 12
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs34612342
MUTYH
0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 11
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 11
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 10