Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10512597
rs10512597
CD300LF ; RAB37
4 17 74703694 intron variant T/A;C snv 0.700 1.000 2 2009 2013
dbSNP: rs1539019
rs1539019
NLRP3
6 0.882 0.240 1 247436999 intron variant A/C snv 0.63 0.700 1.000 2 2009 2011
dbSNP: rs1800789
rs1800789
FGB
4 1.000 0.040 4 154561591 upstream gene variant G/A snv 0.17 0.700 1.000 2 2009 2013
dbSNP: rs2228145
rs2228145
IL6R
57 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.700 1.000 2 2009 2013
dbSNP: rs4129267
rs4129267
IL6R
13 0.807 0.200 1 154453788 intron variant C/G;T snv 0.700 1.000 2 2011 2013
dbSNP: rs6056
rs6056
FGB
3 4 154567669 synonymous variant C/T snv 0.17 0.15 0.700 1.000 2 2009 2011
dbSNP: rs10034922
rs10034922 		3 4 154599476 downstream gene variant G/A snv 5.2E-02 0.700 1.000 1 2011 2011
dbSNP: rs10157379
rs10157379
NLRP3
3 1 247442297 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1016988
rs1016988 		4 5 132408882 upstream gene variant T/C snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs10226084
rs10226084 		3 7 17957989 upstream gene variant T/C snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs1047891
rs1047891
CPS1
34 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 0.700 1.000 1 2009 2009
dbSNP: rs11242111
rs11242111
IRF1-AS1 ; LINC02863
3 5 132420366 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1154988
rs1154988 		7 3 136206349 upstream gene variant T/A snv 0.76 0.700 1.000 1 2013 2013
dbSNP: rs12239046
rs12239046
NLRP3
9 1 247438293 intron variant T/C snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs12511469
rs12511469 		3 4 154530607 downstream gene variant T/A snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs12651106
rs12651106
DCHS2
3 4 154379907 intron variant C/A snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs12712127
rs12712127
IL1R1
3 2 102110201 intron variant A/G snv 0.62 0.700 1.000 1 2013 2013
dbSNP: rs12777
rs12777
SLC22A4 ; MIR3936HG
6 5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02 0.700 1.000 1 2009 2009
dbSNP: rs12915708
rs12915708
SPPL2A
3 15 50756405 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs1476698
rs1476698
FARP2
3 2 241357034 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs16844401
rs16844401
HGFAC
4 1.000 0.040 4 3447925 missense variant G/A;T snv 7.5E-02; 8.3E-06 0.700 1.000 1 2013 2013
dbSNP: rs17690122
rs17690122 		3 5 132532143 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1800787
rs1800787
FGB
4 1.000 0.040 4 154562863 upstream gene variant C/T snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs1800788
rs1800788
FGB
3 4 154562762 upstream gene variant C/T snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs1800790
rs1800790
FGB
9 0.851 0.200 4 154562556 upstream gene variant G/A snv 0.15 0.700 1.000 1 2011 2011