Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 36
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 17
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 12
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 12
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 12
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 12
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 11
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 10
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 9
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 9
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 8
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 8
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 8
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 8
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 7