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: rs1539019
rs1539019
NLRP3
6 0.882 0.240 1 247436999 intron variant A/C snv 0.63 0.800 1.000 2 2009 2011
dbSNP: rs6010044
rs6010044 		3 22 50663510 intergenic variant A/C snv 0.20 0.800 1.000 2 2013 2017
dbSNP: rs150768229
rs150768229
FGB
1 4 154567149 intron variant A/C snv 9.5E-03 0.700 1.000 1 2016 2016
dbSNP: rs1938492
rs1938492 		3 1 65652146 intergenic variant A/C snv 0.43 0.800 1.000 1 2013 2013
dbSNP: rs2227421
rs2227421
FGB
3 4 154571072 3 prime UTR variant A/C snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs10489615
rs10489615
GALNT2
3 1 230169242 intron variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs7004769
rs7004769
LOC157273
1 8 9330085 intron variant A/C;G snv 0.700 1.000 1 2017 2017
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: rs8192284
rs8192284
IL6R
19 0.724 0.720 1 154454494 missense variant A/C;T snv 0.700 1.000 2 2009 2017
dbSNP: rs7518199
rs7518199
IL6R
4 1 154434943 intron variant A/C;T snv 0.39; 4.2E-06 0.700 1.000 1 2011 2011
dbSNP: rs8026198
rs8026198
CAPN3
1 15 42361263 intron variant A/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs6734238
rs6734238 		8 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 0.800 1.000 3 2013 2017
dbSNP: rs12528797
rs12528797
TSBP1-AS1
1 6 32377309 intron variant A/G snv 1.0E-01 0.700 1.000 1 2017 2017
dbSNP: rs12598049
rs12598049
CHD9
1 16 53282942 intron variant A/G snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs12712127
rs12712127
IL1R1
3 2 102110201 intron variant A/G snv 0.62 0.800 1.000 1 2013 2013
dbSNP: rs12915052
rs12915052
SPPL2A
1 15 50732090 intron variant A/G snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs194741
rs194741 		1 14 68821715 intergenic variant A/G snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs2070016
rs2070016
FGA
4 1.000 0.040 4 154589162 intron variant A/G snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs2158177
rs2158177
TH2LCRR
5 0.925 0.120 5 132648366 intron variant A/G snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs2376015
rs2376015 		1 1 65658091 intergenic variant A/G snv 0.43 0.700 1.000 1 2017 2017
dbSNP: rs270607
rs270607
SLC22A4 ; MIR3936HG
3 5 132313493 intron variant A/G snv 0.69 0.700 1.000 1 2011 2011
dbSNP: rs3091307
rs3091307
TH2LCRR
6 0.925 0.160 5 132653444 intron variant A/G snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs367677
rs367677 		1 14 68806373 intergenic variant A/G snv 0.25 0.700 1.000 1 2016 2016
dbSNP: rs6874639
rs6874639
IRF1-AS1
3 5 132443024 intron variant A/G snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs7935829
rs7935829
MS4A6A
3 1.000 0.080 11 60175342 intron variant A/G snv 0.33 0.700 1.000 1 2017 2017