Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 9
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 6
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs9880772 0.827 0.240 3 27736288 intergenic variant G/A snv 0.59 5
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 5
rs4459895
LPP
0.827 0.160 3 188236626 intron variant A/C snv 0.88 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs4240807 0.851 0.160 16 85951755 downstream gene variant A/C snv 0.76 4
rs9392017 0.851 0.160 6 442357 intergenic variant G/A;C snv 4
rs35603048
BMF
0.851 0.160 15 40099764 intron variant C/A;G;T snv 4
rs73005220
CIB3
0.851 0.160 19 16161878 intron variant A/G snv 3.9E-02 4
rs6546149
DTNB
0.851 0.160 2 25406569 intron variant C/G snv 0.38 4
rs2546191
ELL2
0.851 0.160 5 95896837 intron variant G/A snv 0.38 4
rs4525246
GRAMD1B
0.851 0.160 11 123524538 intron variant G/A;C snv 4
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 4
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 4
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs181181503
LOC100507377
0.851 0.160 12 74276187 intron variant T/C snv 1.5E-03 4
rs12711846
MIR4435-2HG ; ACOXL-AS1 ; ACOXL
0.851 0.160 2 111098716 non coding transcript exon variant A/G snv 0.26 4
rs131821
NCAPH2
0.851 0.160 22 50511648 intron variant T/-;TT;TTT;TTTT delins 4
rs11715604
NCK1
0.851 0.160 3 136870707 intron variant A/G;T snv 4
rs2425752
NCOA5
0.851 0.160 20 46073481 intron variant T/C snv 0.79 4
rs2720680
PVT1
0.851 0.160 8 128102971 intron variant A/G snv 0.33 4