Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13088318
FAM172BP
3 101523907 downstream gene variant A/G;T snv 0.24 1
rs1997502
IL1RL2
2 102227789 intron variant A/G;T snv 1
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 1
rs12470864
IL1RL1
0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30 4
rs950881
IL18R1 ; IL1RL1
1.000 0.120 2 102316052 intron variant G/A;T snv 2
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs13001325
IL18R1 ; IL1RL1
1.000 0.040 2 102322576 intron variant C/T snv 0.30 2
rs10865050
IL18R1 ; IL1RL1
2 102324851 intron variant G/A snv 0.18 1
rs12479210
IL1RL1 ; IL18R1
1.000 0.080 2 102332701 intron variant C/A;T snv 1
rs3771180
IL18R1 ; IL1RL1
1.000 0.080 2 102337157 5 prime UTR variant G/A;T snv 1
rs13408661
IL1RL1 ; IL18R1
1.000 0.080 2 102338622 intron variant G/A snv 0.18 1
rs1420101
IL1RL1 ; IL18R1
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 3
rs3771175
IL1RL1 ; IL18R1
0.925 0.080 2 102343750 3 prime UTR variant T/A snv 0.18 1
rs10208293
IL1RL1 ; IL18R1
0.882 0.160 2 102349850 intron variant G/A snv 0.33 2
rs10197862
IL18R1 ; IL1RL1
0.925 0.120 2 102350089 intron variant A/G snv 0.18 2
rs4988958
IL1RL1 ; IL18R1
1.000 0.080 2 102351825 synonymous variant T/C snv 0.34 0.46 1
rs3771166
IL18R1
1.000 0.080 2 102369762 intron variant G/A;T snv 1
rs10883723
MFSD13A ; ACTR1A
10 102466075 5 prime UTR variant T/C snv 0.29 1
rs1468788
SLC9A4
1.000 0.080 2 102476054 intron variant C/T snv 0.54 1
rs201333164
SUFU
10 102518505 intron variant GTCT/-;GTCTGTCT;GTCTGTCTGTCT delins 6.7E-04 1
rs227275
MANBA
4 102672741 intron variant A/C snv 0.55 1
rs9989163 14 102768675 downstream gene variant G/A snv 0.45 1
rs616402
PEX14
1 10506215 intron variant C/T snv 0.29 1
rs2056417
PEX14
1 10521601 intron variant G/A snv 0.25 1
rs12045923
PEX14
1 10583772 intron variant C/G;T snv 1