Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 7
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 5
rs12777
MIR3936HG ; SLC22A4
5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02 4
rs59950280
LOC105374354
4 3450618 upstream gene variant G/A snv 0.41 4
rs2710804 7 36044919 intron variant T/C snv 0.29 3
rs7588285
COLEC11
2 3600596 intron variant C/G;T snv 3
rs7916868
JMJD1C
10 63229171 intron variant A/T snv 0.47 3
rs1016988 5 132408882 upstream gene variant T/C snv 0.20 2
rs10489615
GALNT2
1 230169242 intron variant A/C;G snv 2
rs10512597
RAB37 ; CD300LF
17 74703694 intron variant T/A;C snv 2
rs1521516
DIP2B
12 50661925 intron variant C/T snv 0.27 2
rs2522056
IRF1-AS1
5 132466034 intron variant G/A snv 0.25 2
rs7012814 8 9315848 intron variant G/A;T snv 2
rs7873907 9 89610568 downstream gene variant T/C snv 0.48 2
rs1012793
IRF1-AS1
5 132445653 intron variant G/A;C snv 1
rs10157379
NLRP3
1 247442297 intron variant C/G;T snv 1
rs1019670
MS4A6A
11 60173126 missense variant T/A snv 1
rs10226084 7 17957989 upstream gene variant T/C snv 0.46 1
rs1029738
LOC112267993
7 22834428 downstream gene variant C/A snv 0.23 1
rs1035560
PKD1L3
16 71998831 intron variant T/A;C snv 0.38 1
rs10479002
MIR3936HG ; SLC22A4
5 132335969 synonymous variant C/G snv 1
rs10761756
JMJD1C
10 63412568 intron variant C/T snv 0.42 1
rs10864726
GALNT2
1 230160406 intron variant C/T snv 0.45 1
rs10950690
SNX13
7 17941687 non coding transcript exon variant C/A;G snv 1