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: rs10494326
rs10494326 		1 1 159679910 intergenic variant C/T snv 5.3E-02 0.800 1.000 3 2012 2019
dbSNP: rs11265257
rs11265257 		1 1 159699194 intergenic variant C/T snv 0.34 0.700 1.000 3 2012 2013
dbSNP: rs11265260
rs11265260 		2 1.000 0.080 1 159730249 intergenic variant A/G snv 6.8E-02 0.800 1.000 3 2012 2019
dbSNP: rs12081252
rs12081252 		1 1 159736723 intergenic variant T/C snv 7.6E-02 0.700 1.000 3 2012 2014
dbSNP: rs12081264
rs12081264 		1 1 159736770 intergenic variant T/C snv 0.15 0.700 1.000 3 2012 2014
dbSNP: rs12239046
rs12239046
NLRP3
9 1 247438293 intron variant T/C snv 0.58 0.800 1.000 3 2011 2019
dbSNP: rs1470515
rs1470515 		1 1 159683809 intergenic variant C/T snv 0.36 0.700 1.000 3 2012 2013
dbSNP: rs16842502
rs16842502 		1 1 159684073 intergenic variant C/A snv 5.5E-02 0.700 1.000 3 2012 2014
dbSNP: rs16842568
rs16842568 		1 1 159706430 upstream gene variant A/G snv 5.6E-02 0.700 1.000 3 2012 2014
dbSNP: rs16842599
rs16842599 		1 1 159727685 intergenic variant T/C snv 7.4E-02 0.700 1.000 3 2012 2014
dbSNP: rs1892534
rs1892534
LEPR
7 0.925 0.120 1 65640261 3 prime UTR variant C/T snv 0.44 0.800 1.000 3 2008 2019
dbSNP: rs2228145
rs2228145
IL6R
57 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.800 1.000 3 2008 2019
dbSNP: rs2244608
rs2244608
HNF1A ; HNF1A-AS1
9 0.882 0.160 12 120979185 intron variant A/G snv 0.29 0.700 1.000 3 2012 2013
dbSNP: rs2464196
rs2464196
HNF1A
17 0.742 0.320 12 120997624 missense variant G/A snv 0.34 0.27 0.700 1.000 3 2013 2014
dbSNP: rs2592887
rs2592887 		1 1 159683149 intergenic variant C/T snv 0.43 0.700 1.000 3 2012 2013
dbSNP: rs2650000
rs2650000
HNF1A-AS1
10 0.851 0.200 12 120951159 intron variant A/C snv 0.70 0.800 1.000 3 2012 2019
dbSNP: rs2808624
rs2808624 		1 1 159696131 intergenic variant C/G;T snv 0.700 1.000 3 2012 2013
dbSNP: rs2836878
rs2836878 		7 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 0.800 1.000 3 2011 2019
dbSNP: rs3093059
rs3093059
CRP
11 0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 0.800 1.000 3 2011 2019
dbSNP: rs3093075
rs3093075 		5 0.882 0.120 1 159710123 upstream gene variant G/T snv 0.13 0.700 1.000 3 2012 2014
dbSNP: rs3093077
rs3093077 		9 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 0.700 1.000 3 2012 2014
dbSNP: rs4537545
rs4537545
IL6R
11 0.790 0.160 1 154446403 intron variant C/T snv 0.48 0.800 1.000 3 2009 2019
dbSNP: rs6700896
rs6700896
LEPR
9 0.827 0.160 1 65624099 intron variant C/T snv 0.44 0.800 1.000 3 2009 2019
dbSNP: rs780094
rs780094
GCKR
62 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 3 2008 2019
dbSNP: rs7979473
rs7979473
HNF1A
2 12 120982457 intron variant A/C;G snv 0.800 1.000 3 2012 2019