Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 10
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 7
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 5
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 5
rs7422339
CPS1
1.000 0.080 2 210675783 missense variant C/A snv 5
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 4
rs61812598
IL6R
1.000 0.080 1 154447611 intron variant G/A snv 0.31 4
rs59950280
LOC105374354
4 3450618 upstream gene variant G/A snv 0.41 4
rs12777
MIR3936HG ; SLC22A4
5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02 4
rs2710804 7 36044919 intron variant T/C snv 0.29 3
rs7588285
COLEC11
2 3600596 intron variant C/G;T snv 3
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 3
rs7916868
JMJD1C
10 63229171 intron variant A/T snv 0.47 3
rs1892534
LEPR
0.925 0.120 1 65640261 3 prime UTR variant C/T snv 0.44 3
rs7935829
MS4A6A
1.000 0.080 11 60175342 intron variant A/G snv 0.33 3
rs1016988 5 132408882 upstream gene variant T/C snv 0.20 2
rs2801231 1.000 0.080 X 122083259 intergenic variant T/A;C;G snv 2
rs7012814 8 9315848 intron variant G/A;T snv 2
rs7873907 9 89610568 downstream gene variant T/C snv 0.48 2