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: rs2794520
rs2794520 		9 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 0.800 1.000 8 2007 2019
dbSNP: rs7553007
rs7553007 		7 0.827 0.120 1 159728759 intergenic variant G/A snv 0.31 0.800 1.000 8 2009 2019
dbSNP: rs4420638
rs4420638
APOC1
43 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.800 1.000 7 2009 2019
dbSNP: rs1183910
rs1183910
HNF1A
5 1.000 0.080 12 120983004 intron variant G/A snv 0.28 0.800 1.000 6 2009 2019
dbSNP: rs1341665
rs1341665 		2 1.000 0.080 1 159721769 intergenic variant G/A snv 0.32 0.800 1.000 6 2012 2019
dbSNP: rs7310409
rs7310409
HNF1A
7 0.925 0.160 12 120987058 intron variant A/C;G;T snv 0.800 1.000 6 2008 2019
dbSNP: rs1205
rs1205
CRP
46 0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 0.700 1.000 5 2012 2014
dbSNP: rs12068753
rs12068753 		2 1.000 0.120 1 159722747 intergenic variant T/A snv 0.15 0.800 1.000 5 2012 2015
dbSNP: rs6734238
rs6734238 		8 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 0.800 1.000 5 2011 2019
dbSNP: rs7953249
rs7953249
HNF1A-AS1
4 0.882 0.160 12 120965921 splice region variant G/A snv 0.59 0.800 1.000 5 2012 2019
dbSNP: rs1169310
rs1169310
HNF1A ; C12orf43
3 12 121001630 3 prime UTR variant G/A snv 0.31 0.800 1.000 4 2008 2019
dbSNP: rs16842559
rs16842559 		1 1 159706381 upstream gene variant T/C snv 5.6E-02 0.800 1.000 4 2012 2019
dbSNP: rs2027471
rs2027471 		1 1 159719598 intergenic variant T/A snv 0.32 0.700 1.000 4 2012 2014
dbSNP: rs2393791
rs2393791
HNF1A
8 0.925 0.160 12 120986153 intron variant C/T snv 0.62 0.800 1.000 4 2013 2019
dbSNP: rs2808628
rs2808628 		2 1 159706221 upstream gene variant G/A snv 0.31 0.700 1.000 4 2012 2014
dbSNP: rs2808629
rs2808629 		3 0.925 0.160 1 159707006 upstream gene variant G/A snv 0.31 0.700 1.000 4 2012 2014
dbSNP: rs3091244
rs3091244
CRP
17 0.724 0.280 1 159714875 upstream gene variant G/A;T snv 0.800 1.000 4 2008 2018
dbSNP: rs4129267
rs4129267
IL6R
13 0.807 0.200 1 154453788 intron variant C/G;T snv 0.800 1.000 4 2011 2019
dbSNP: rs7305618
rs7305618
HNF1A-AS1
3 0.925 0.160 12 120965129 intron variant C/T snv 0.28 0.800 1.000 4 2012 2019
dbSNP: rs876537
rs876537
CRPP1
3 1.000 0.080 1 159705143 non coding transcript exon variant C/T snv 0.34 0.800 1.000 4 2012 2019
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