Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4406273
LOC112267902 ; HLA-B ; LINC02571
0.925 0.040 6 31298313 intron variant G/A snv 8.6E-02 2
rs7709212
LOC285626
0.925 0.040 5 159337169 intron variant T/C snv 0.34 2
rs4685408
PLCL2
0.925 0.040 3 16954543 intron variant G/A snv 0.56 2
rs892085
QTRT1
0.925 0.040 19 10707416 intron variant G/A snv 0.57 0.59 2
rs1056198
RNF114
0.925 0.040 20 49939692 intron variant C/T snv 0.34 2
rs7536201
RUNX3
0.925 0.040 1 24966593 upstream gene variant T/C;G snv 2
rs2066819
STAT2
0.925 0.040 12 56356420 intron variant C/T snv 4.9E-02 4.5E-02 2
rs12445568
STX1B
0.925 0.040 16 30993491 splice region variant T/C snv 0.39 0.38 2
rs610604
TNFAIP3
0.827 0.240 6 137878280 intron variant G/T snv 0.58 2
rs2233278
TNIP1
0.925 0.040 5 151087628 5 prime UTR variant G/C;T snv 4.8E-02 2
rs181359
UBE2L3
0.882 0.080 22 21574352 intron variant G/A snv 0.21 2
rs2675669 1.000 0.040 10 73894114 intergenic variant C/T snv 0.55 1
rs4649203 0.851 0.160 1 24193430 intergenic variant G/A snv 0.61 1
rs4722404 0.851 0.120 7 3089155 intron variant T/C snv 0.40 1
rs4845454 0.925 0.040 1 152619708 downstream gene variant C/A;T snv 1
rs6474412 0.925 0.120 8 42695355 upstream gene variant C/T snv 0.64 1
rs12489120
BHLHE40 ; BHLHE40-AS1
1.000 0.040 3 4978778 intron variant C/A;G;T snv 1
rs11652075
CARD14 ; SGSH
0.882 0.040 17 80205094 missense variant C/T snv 0.41 0.40 1
rs4712528
CDKAL1
1.000 0.040 6 20678199 intron variant G/C;T snv 1
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 1
rs27524
ERAP1 ; CAST
0.851 0.160 5 96766240 intron variant A/G snv 0.61 1
rs3135388
HLA-DRA
0.807 0.240 6 32445274 downstream gene variant A/G snv 0.90 1
rs9394026
MUC22
1.000 0.040 6 31014767 intron variant G/A snv 0.24 1