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: rs4506565
rs4506565
TCF7L2
22 0.790 0.280 10 112996282 intron variant A/G;T snv 0.870 0.900 10 2006 2020
dbSNP: rs5215
rs5215
KCNJ11
7 0.827 0.160 11 17387083 missense variant C/T snv 0.64 0.71 0.860 0.941 17 2007 2018
dbSNP: rs12779790
rs12779790 		5 0.882 0.120 10 12286011 intergenic variant A/G snv 0.17 0.850 1.000 8 2008 2015
dbSNP: rs114202595
rs114202595
PAX4
4 0.882 0.120 7 127614533 missense variant G/A;T snv 1.2E-04; 9.1E-06 0.850 1.000 7 2001 2013
dbSNP: rs1800574
rs1800574
HNF1A ; HNF1A-AS1
6 0.882 0.080 12 120979061 missense variant C/T snv 2.9E-02 2.2E-02 0.850 0.857 7 2004 2018
dbSNP: rs10886471
rs10886471
GRK5
1 1.000 0.080 10 119389891 intron variant C/T snv 0.39 0.850 1.000 5 2013 2018
dbSNP: rs231362
rs231362
KCNQ1 ; KCNQ1OT1
1 1.000 0.080 11 2670241 non coding transcript exon variant A/G snv 0.62 0.840 1.000 10 2010 2019
dbSNP: rs4607103
rs4607103
ADAMTS9-AS2
4 0.882 0.120 3 64726228 intron variant C/T snv 0.28 0.840 1.000 9 2008 2019
dbSNP: rs7578597
rs7578597
THADA
7 0.807 0.240 2 43505684 missense variant T/C snv 9.9E-02 0.14 0.840 1.000 9 2008 2017
dbSNP: rs7612463
rs7612463
UBE2E2
3 0.925 0.080 3 23294959 intron variant C/A;G snv 0.840 0.889 9 2010 2018
dbSNP: rs11708067
rs11708067
ADCY5
9 0.882 0.080 3 123346931 intron variant A/G snv 0.19 0.840 0.875 8 2010 2018
dbSNP: rs12970134
rs12970134 		13 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 0.840 1.000 8 2009 2018
dbSNP: rs972283
rs972283
LOC105375508
3 1.000 0.080 7 130782095 intergenic variant A/G;T snv 0.840 1.000 8 2010 2016
dbSNP: rs6815464
rs6815464
MAEA
2 0.925 0.120 4 1316113 intron variant C/G;T snv 0.840 1.000 7 2011 2019
dbSNP: rs7961581
rs7961581
TSPAN8
7 0.827 0.200 12 71269322 intron variant C/T snv 0.75 0.840 1.000 6 2008 2017
dbSNP: rs9300039
rs9300039 		4 0.851 0.160 11 41893816 intergenic variant C/A snv 9.8E-02 0.840 1.000 6 2007 2011
dbSNP: rs515071
rs515071
ANK1 ; MIR486-1
1 1.000 0.080 8 41661944 splice region variant A/G;T snv 0.78 0.840 1.000 4 2012 2017
dbSNP: rs340874
rs340874
PROX1 ; PROX1-AS1
7 0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 0.830 1.000 8 2010 2019
dbSNP: rs4712523
rs4712523
CDKAL1
3 0.925 0.120 6 20657333 intron variant A/G snv 0.41 0.830 1.000 7 2009 2019
dbSNP: rs4812829
rs4812829
HNF4A
3 0.925 0.120 20 44360627 intron variant G/A snv 0.18 0.830 1.000 7 2011 2017
dbSNP: rs9465871
rs9465871
CDKAL1
4 0.882 0.120 6 20717024 intron variant T/C snv 0.30 0.830 1.000 6 2007 2017
dbSNP: rs1535500
rs1535500
KCNK16 ; KCNK17 ; LOC105375047
1 1.000 0.080 6 39316274 missense variant G/T snv 0.51 0.60 0.830 1.000 5 2011 2019
dbSNP: rs831571
rs831571 		1 1.000 0.080 3 64062621 intergenic variant T/C snv 0.81 0.830 1.000 5 2011 2019
dbSNP: rs1799884
rs1799884
GCK
6 1.000 0.080 7 44189469 intron variant C/T snv 0.17 0.830 0.750 4 2008 2013
dbSNP: rs3802177
rs3802177
SLC30A8 ; LOC105375716
5 1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 0.820 1.000 10 2008 2019