Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111668293
TBX15
0.807 0.080 1 118896200 intron variant G/- del 0.12 7
rs7542354
C1orf127
0.807 0.080 1 10980328 intron variant G/A snv 0.37 7
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs760077
MTX1 ; THBS3
0.925 0.120 1 155208991 missense variant T/A snv 0.36 7
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 7
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 7
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 7
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs34599082
ACKR1 ; CADM3-AS1
1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 7
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 7
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 7
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 6
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 6
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84 6
rs6426833 0.827 0.120 1 19845367 TF binding site variant G/A snv 0.52 6
rs3766606
PARK7
0.827 0.120 1 7962137 intron variant G/T snv 0.22 6
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 6
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs2474937 0.851 0.120 1 118360355 intergenic variant A/G snv 0.25 6