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: rs4560142
rs4560142 		2 2 21160845 intergenic variant C/T snv 0.75 0.700 1.000 1 2008 2008
dbSNP: rs4591370
rs4591370 		3 2 21160870 intergenic variant A/G snv 0.75 0.700 1.000 1 2008 2008
dbSNP: rs4605275
rs4605275 		3 1.000 0.080 19 44835236 intergenic variant T/C snv 0.69 0.700 1.000 1 2008 2008
dbSNP: rs478442
rs478442 		18 0.851 0.120 2 21176344 intergenic variant G/C;T snv 0.700 1.000 1 2008 2008
dbSNP: rs488507
rs488507 		2 2 21170817 intergenic variant G/T snv 0.78 0.700 1.000 1 2008 2008
dbSNP: rs506585
rs506585 		4 2 21174310 intergenic variant G/A;C;T snv 0.700 1.000 1 2008 2008
dbSNP: rs538928
rs538928 		2 2 21166147 intergenic variant A/G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs576203
rs576203 		2 2 21170751 intergenic variant A/G snv 0.76 0.700 1.000 1 2008 2008
dbSNP: rs6589566
rs6589566
ZPR1
10 0.882 0.080 11 116781707 intron variant G/A;C;T snv 0.700 1.000 1 2008 2008
dbSNP: rs7703051
rs7703051 		18 0.851 0.120 5 75329662 intron variant C/A snv 0.38 0.700 1.000 1 2008 2008
dbSNP: rs780094
rs780094
GCKR
62 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2008 2008
dbSNP: rs10401969
rs10401969
SUGP1
25 0.776 0.240 19 19296909 intron variant T/C snv 0.10 0.700 1.000 5 2009 2013
dbSNP: rs12670798
rs12670798
DNAH11 ; LOC105375183
5 1.000 0.040 7 21567734 intron variant T/C snv 0.26 0.700 1.000 3 2009 2013
dbSNP: rs157580
rs157580
TOMM40
14 0.882 0.160 19 44892009 intron variant G/A snv 0.69 0.700 1.000 3 2009 2012
dbSNP: rs174546
rs174546
FADS1 ; FADS2
17 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 0.700 1.000 3 2009 2013
dbSNP: rs3846662
rs3846662
HMGCR
12 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.700 1.000 3 2009 2013
dbSNP: rs515135
rs515135 		9 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 0.700 1.000 3 2009 2013
dbSNP: rs6544713
rs6544713
ABCG8
5 0.925 0.040 2 43846742 non coding transcript exon variant T/C snv 0.75 0.700 1.000 2 2009 2013
dbSNP: rs1501908
rs1501908 		5 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs174570
rs174570
FADS2
11 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs2650000
rs2650000
HNF1A-AS1
10 0.851 0.200 12 120951159 intron variant A/C snv 0.70 0.700 1.000 1 2009 2009
dbSNP: rs3846663
rs3846663
HMGCR ; CERT1
7 0.882 0.120 5 75359901 intron variant C/T snv 0.35 0.700 1.000 1 2009 2009
dbSNP: rs4844614
rs4844614
CR1L
3 1.000 0.040 1 207701830 intron variant G/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs5031002
rs5031002
AR
3 1.000 0.040 X 67722783 intron variant G/A snv 1.5E-02 1.5E-02 0.700 1.000 1 2009 2009
dbSNP: rs6102059
rs6102059
LOC102724968
3 1.000 0.040 20 40600144 intergenic variant C/T snv 0.33 0.700 1.000 1 2009 2009