Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs616402
PEX14
1 10506215 intron variant C/T snv 0.29 1
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs12470864
IL1RL1
0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30 4
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs74847330
ARHGAP15
2 143074030 intergenic variant A/G snv 8.8E-02 4
rs1057258
INPP5D
2 233206983 3 prime UTR variant C/T snv 0.30 3
rs1420101
IL1RL1 ; IL18R1
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 3
rs2164068
PLCL1
1.000 0.120 2 198079128 intron variant T/A snv 0.52 3
rs1017494 1.000 0.080 2 234770601 regulatory region variant C/A;G;T snv 2
rs10174949
LINC00299
1.000 0.080 2 8302118 non coding transcript exon variant G/A snv 0.23 2
rs10197862
IL18R1 ; IL1RL1
0.925 0.120 2 102350089 intron variant A/G snv 0.18 2
rs10208293
IL1RL1 ; IL18R1
0.882 0.160 2 102349850 intron variant G/A snv 0.33 2
rs1064213
PLCL1
2 198085516 missense variant G/A snv 0.44 0.41 2
rs11684176
PLCL1
2 198090050 intron variant C/T snv 0.38 2
rs13001325
IL18R1 ; IL1RL1
1.000 0.040 2 102322576 intron variant C/T snv 0.30 2
rs13416555
LINC00299
1.000 0.080 2 8301605 intron variant C/A;G snv 2
rs1595824
PLCL1
2 198009282 intron variant C/A;T snv 2
rs346835
LINC00299
2 8298563 intron variant C/T snv 0.39 2
rs367023
LINC00299
1.000 0.040 2 8309993 intron variant A/G snv 0.35 2
rs3856439
LINC00299
0.925 0.080 2 8319274 intron variant C/A;T snv 0.29 2
rs4850808 2 197711418 intron variant T/A;C snv 2
rs6738825
PLCL1
0.851 0.200 2 198032171 intron variant A/G snv 0.49 2
rs7562
FOSL2
2 28412873 3 prime UTR variant T/C snv 0.53 2
rs891058
LINC00299
1.000 0.040 2 8302417 non coding transcript exon variant G/A snv 0.23 2
rs950881
IL18R1 ; IL1RL1
1.000 0.120 2 102316052 intron variant G/A;T snv 2