Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 5
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 4
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 3
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 3
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 3
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 3
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 2
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 2
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 2
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 2
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 2
rs725613
CLEC16A
0.851 0.240 16 11075826 intron variant T/G snv 0.42 2
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 2
rs3891175
HLA-DQB1
0.851 0.160 6 32666690 5 prime UTR variant C/T snv 0.20 2
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 2
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 2
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 2