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
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 12
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 12
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 12
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs17102823 0.776 0.080 14 34894698 intergenic variant A/C;G snv 10
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 9
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 9
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 8
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 8
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 8
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 8
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 8
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 8