Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1012793
IRF1-AS1
5 132445653 intron variant G/A;C snv 1
rs10157379
NLRP3
1 247442297 intron variant C/G;T snv 1
rs1016988 5 132408882 upstream gene variant T/C snv 0.20 2
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
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs10479002
MIR3936HG ; SLC22A4
5 132335969 synonymous variant C/G snv 1
rs10489615
GALNT2
1 230169242 intron variant A/C;G snv 2
rs10512597
RAB37 ; CD300LF
17 74703694 intron variant T/A;C snv 2
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 4
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
rs11102001
GSTM5 ; EPS8L3
0.925 0.080 1 109757069 missense variant G/A snv 9.4E-02 0.16 2
rs11136252
SPATC1 ; PARP10
8 144010325 intron variant T/C snv 0.45 1
rs11230201
MS4A4E ; MS4A4A
1.000 0.080 11 60229521 intron variant C/G;T snv 1
rs11242111
LINC02863 ; IRF1-AS1
5 132420366 intron variant A/G;T snv 1
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 5
rs11630054
SPPL2A
15 50723495 intron variant T/G snv 0.30 1
rs11780978
PLEC
1.000 0.040 8 143960684 intron variant G/A snv 0.30 2
rs11859517
CHD9
16 53147335 intron variant C/T snv 0.28 1
rs11864453
DHODH
16 72016581 non coding transcript exon variant C/T snv 0.39 1
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 7