Source: INFERRED ×
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 73
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 30
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 19
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 12
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 12
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 12
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 9
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 7
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 7
rs6054
FGB
1.000 0.080 4 154568456 missense variant C/T snv 2.4E-03 2.7E-03 6
rs12777
MIR3936HG ; SLC22A4
5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02 6
rs7681423 4 154621096 intergenic variant C/T snv 0.26 5
rs7422339
CPS1
1.000 0.080 2 210675783 missense variant C/A snv 5
rs6050
FGA
0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 5
rs2066861
FGG
4 154606284 intron variant C/T snv 0.26 5
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 5
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 5
rs1016988 5 132408882 upstream gene variant T/C snv 0.20 4
rs148685782
FGG
1.000 0.080 4 154611883 missense variant G/C snv 1.9E-03 2.2E-03 4
rs16844401
HGFAC
1.000 0.040 4 3447925 missense variant G/A;T snv 7.5E-02; 8.3E-06 4
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs61812598
IL6R
1.000 0.080 1 154447611 intron variant G/A snv 0.31 4
rs7518199
IL6R
1 154434943 intron variant A/C;T snv 0.39; 4.2E-06 4
rs7529229
IL6R
0.851 0.120 1 154448302 intron variant T/C snv 0.48 4