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: 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: 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: 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: 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
dbSNP: rs9987289
rs9987289
LOC157273
10 1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 0.800 1.000 3 2011 2019
dbSNP: rs10521222
rs10521222 		1 16 51124799 intergenic variant C/T snv 3.2E-02 0.800 1.000 2 2011 2018
dbSNP: rs10745954
rs10745954
C12orf42
1 12 103089316 intron variant A/G snv 0.60 0.800 1.000 2 2011 2019
dbSNP: rs10889569
rs10889569
LEPR
1 1 65620511 intron variant A/T snv 0.46 0.800 1.000 2 2013 2019
dbSNP: rs1160985
rs1160985
TOMM40
6 1.000 0.080 19 44900155 intron variant C/T snv 0.52 0.800 1.000 2 2012 2019
dbSNP: rs12741825
rs12741825 		3 1 159700355 downstream gene variant C/T snv 0.24 0.800 1.000 2 2012 2013
dbSNP: rs12749227
rs12749227 		1 1 159689319 intergenic variant C/T snv 0.25 0.800 1.000 2 2012 2018
dbSNP: rs12755606
rs12755606 		2 1 159700546 downstream gene variant C/G snv 0.24 0.800 1.000 2 2012 2016
dbSNP: rs13233571
rs13233571
BCL7B
5 0.925 0.120 7 73556901 intron variant C/T snv 9.2E-02 0.800 1.000 2 2011 2018
dbSNP: rs1800947
rs1800947
CRP
28 0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 0.800 1.000 2 2013 2018
dbSNP: rs3093068
rs3093068 		3 1.000 0.040 1 159711574 downstream gene variant G/C snv 0.13 0.800 1.000 2 2013 2018
dbSNP: rs3845624
rs3845624 		2 1 159248476 regulatory region variant A/C snv 0.57 0.800 1.000 2 2012 2019
dbSNP: rs4420065
rs4420065 		1 1 65695778 intergenic variant T/C snv 0.58 0.800 1.000 2 2011 2019
dbSNP: rs643434
rs643434
ABO
8 9 133266942 intron variant A/G;T snv 0.800 1.000 2 2012 2018
dbSNP: rs6857
rs6857
NECTIN2
16 0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 0.800 1.000 2 2013 2019
dbSNP: rs726640
rs726640 		1 1 159685728 intergenic variant G/A;T snv 0.800 1.000 2 2012 2019
dbSNP: rs769449
rs769449
APOE
11 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 0.800 1.000 2 2008 2019