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: rs12425791
rs12425791 		4 0.882 0.120 12 674318 downstream gene variant G/A;C snv 0.100 0.857 14 2009 2019
dbSNP: rs11833579
rs11833579 		6 0.827 0.200 12 666033 upstream gene variant G/A snv 0.25 0.100 0.846 13 2011 2019
dbSNP: rs397507444
rs397507444
MTHFR
306 0.405 0.880 1 11794407 missense variant T/G snv 0.100 0.909 11 2006 2018
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
44 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.080 0.875 8 2010 2020
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.060 0.833 6 2010 2019
dbSNP: rs3918242
rs3918242
MMP9
54 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.060 1.000 6 2015 2020
dbSNP: rs662799
rs662799
APOA5
33 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.060 1.000 6 2012 2018
dbSNP: rs1800896
rs1800896
IL10 ; IL19
113 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.050 0.800 5 2010 2020
dbSNP: rs3093059
rs3093059
CRP
11 0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 0.050 1.000 5 2013 2020
dbSNP: rs6025
rs6025
F5
43 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.740 0.400 5 1996 2016
dbSNP: rs966221
rs966221
PDE4D
2 1.000 0.080 5 60206693 intron variant A/G snv 0.57 0.050 0.800 5 2005 2020
dbSNP: rs17222919
rs17222919
ALOX5AP
2 1.000 0.080 13 30734192 intron variant T/A;G snv 0.040 0.750 4 2011 2019
dbSNP: rs1800796
rs1800796
IL6 ; STEAP1B ; IL6-AS1
74 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.040 1.000 4 2011 2017
dbSNP: rs2200733
rs2200733 		12 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 0.730 0.750 4 2008 2016
dbSNP: rs2383207
rs2383207
CDKN2B-AS1
22 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.040 0.750 4 2013 2020
dbSNP: rs10033464
rs10033464 		8 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 0.030 0.667 3 2008 2016
dbSNP: rs1024611
rs1024611 		63 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.030 0.667 3 2010 2015
dbSNP: rs10507391
rs10507391
ALOX5AP
10 0.776 0.320 13 30737959 intron variant A/T snv 0.52 0.030 0.667 3 2015 2019
dbSNP: rs10744777
rs10744777
ALDH2
1 1.000 0.080 12 111795214 intron variant T/C snv 0.53 0.720 1.000 3 2014 2018
dbSNP: rs10757274
rs10757274
CDKN2B-AS1
22 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.030 1.000 3 2009 2019
dbSNP: rs10947803
rs10947803
KCNK17
2 1.000 0.080 6 39302834 intron variant C/A snv 0.030 1.000 3 2010 2014
dbSNP: rs1205
rs1205
CRP
46 0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 0.030 1.000 3 2006 2020
dbSNP: rs12188950
rs12188950
PDE4D ; PART1
2 0.925 0.120 5 60487490 intron variant C/T snv 0.13 0.030 1.000 3 2008 2017
dbSNP: rs1501299
rs1501299
ADIPOQ ; ADIPOQ-AS1
52 0.597 0.720 3 186853334 intron variant G/C;T snv 0.030 < 0.001 3 2006 2015
dbSNP: rs1799963
rs1799963
F2
25 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.720 1.000 3 2015 2016