Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10174949
LINC00299
1.000 0.080 2 8302118 non coding transcript exon variant G/A snv 0.23 1
rs10176664
IL18R1
2 102359712 intron variant G/A;C snv 1
rs10176820
IL18RAP
2 102437960 intron variant T/C snv 0.24 1
rs10177758
PLCL1
2 197994193 intron variant A/G snv 0.48 1
rs10178214
IL1RL2
2 102242461 downstream gene variant G/T snv 0.24 1
rs10178845
LINC00299
1.000 0.080 2 8303673 intron variant G/A snv 0.23 1
rs10181785 2 102408814 upstream gene variant C/T snv 0.22 1
rs10184227
PLCL1
2 198029581 intron variant C/T snv 0.48 1
rs10184395
PLCL1
2 198029561 intron variant G/A snv 0.69 1
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 2
rs10189897
PLCL1
2 197948686 intron variant A/G;T snv 1
rs10190226
PLCL1
2 198036840 intron variant C/T snv 0.69 1
rs10192157
IL18R1 ; IL1RL1
1.000 0.080 2 102351896 missense variant C/T snv 0.34 0.46 2
rs10192466
PLCL1
2 197873295 intron variant G/A;C snv 1
rs10196612
PLCL1
2 198029415 intron variant T/C snv 0.49 1
rs10196961
RFTN2
2 197649206 intron variant G/A snv 0.47 1
rs10197310 2 102403570 downstream gene variant T/A snv 0.22 1
rs10197862
IL18R1 ; IL1RL1
0.925 0.120 2 102350089 intron variant A/G snv 0.18 2
rs10198606
PLCL1
2 197905015 intron variant C/A;G;T snv 1
rs10202813 2 102403280 downstream gene variant G/T snv 0.22 1
rs10206714
PLCL1
2 198041757 intron variant C/A;T snv 1
rs10206753
IL18R1 ; IL1RL1
1.000 0.080 2 102351902 missense variant T/C;G snv 0.34; 4.0E-06 2
rs10207433
PLCL1
2 197941206 intron variant G/T snv 0.51 1
rs10208293
IL1RL1 ; IL18R1
0.882 0.160 2 102349850 intron variant G/A snv 0.33 1
rs10210006
LINC00299
2 8326356 intron variant C/G snv 0.29 1