Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35741374
LINC01185
1.000 0.040 2 60845432 intron variant C/T snv 0.64 1
rs4243971 0.827 0.120 20 32261714 intergenic variant T/G snv 0.64 6
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs469758
LOC102724748 ; ERAP1
0.827 0.120 5 96786011 intron variant C/T snv 0.62 0.63 5
rs4363385
LOC105371446
0.925 0.120 1 153016845 upstream gene variant T/C snv 0.62 2
rs1870293
SETD1A
0.827 0.120 16 30959620 intron variant T/C snv 0.62 5
rs118086960
CFL1
1.000 0.040 11 65825973 intron variant A/T snv 0.62 1
rs27524
ERAP1 ; CAST
0.851 0.160 5 96766240 intron variant A/G snv 0.61 1
rs1405108 0.827 0.120 2 198880294 downstream gene variant C/A snv 0.61 5
rs2538470 0.827 0.120 7 148523356 intergenic variant A/G snv 0.61 6
rs4649203 0.851 0.160 1 24193430 intergenic variant G/A snv 0.61 1
rs6590334
ETS1
1.000 0.040 11 128533313 intron variant T/C snv 0.60 1
rs9687958 0.827 0.120 5 40496321 intron variant G/T snv 0.60 5
rs8016947 0.925 0.080 14 35363460 intron variant T/G snv 0.60 1
rs2700987
ELMO1
1.000 0.040 7 37346633 intron variant C/A snv 0.60 1
rs892085
QTRT1
0.925 0.040 19 10707416 intron variant G/A snv 0.57 0.59 2
rs6693105 0.827 0.120 1 152618187 downstream gene variant T/C snv 0.59 5
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 1
rs7404095
PRKCB
0.827 0.120 16 23853269 intron variant T/C snv 0.58 6
rs7042370
LURAP1L-AS1 ; LURAP1L
0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs2234161
TNFRSF14
0.827 0.120 1 2559766 non coding transcript exon variant C/T snv 4.1E-05; 0.55 0.58 5
rs610604
TNFAIP3
0.827 0.240 6 137878280 intron variant G/T snv 0.58 2
rs1992661 0.827 0.120 5 40414887 upstream gene variant G/A snv 0.58 5
rs2026029
FNDC3A
0.827 0.120 13 49021195 intron variant A/G snv 0.58 5
rs1581803 1.000 0.040 1 152619805 downstream gene variant G/T snv 0.58 1