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: rs13266634
rs13266634
SLC30A8 ; LOC105375716
23 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 1.000 0.973 75 2007 2019
dbSNP: rs4402960
rs4402960
IGF2BP2
21 0.724 0.400 3 185793899 intron variant G/T snv 0.38 1.000 0.977 44 2007 2018
dbSNP: rs7903146
rs7903146
TCF7L2
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.900 0.953 190 2006 2020
dbSNP: rs1801282
rs1801282
PPARG
131 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.900 0.902 122 1997 2018
dbSNP: rs12255372
rs12255372
TCF7L2
28 0.667 0.480 10 113049143 intron variant G/A;T snv 0.900 0.908 65 2006 2020
dbSNP: rs5219
rs5219
KCNJ11
25 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 0.900 0.906 64 1998 2019
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.900 0.961 51 2007 2019
dbSNP: rs10811661
rs10811661 		22 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 0.900 0.955 44 2007 2019
dbSNP: rs1111875
rs1111875 		10 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 0.900 0.914 35 2007 2020
dbSNP: rs10830963
rs10830963
MTNR1B
27 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.900 0.939 33 2009 2020
dbSNP: rs2237892
rs2237892
KCNQ1
16 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 0.900 1.000 32 2008 2019
dbSNP: rs7756992
rs7756992
CDKAL1
12 0.827 0.240 6 20679478 intron variant A/G;T snv 0.900 0.966 29 2007 2019
dbSNP: rs8050136
rs8050136
FTO
32 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.900 0.964 28 2007 2019
dbSNP: rs1470579
rs1470579
IGF2BP2
5 0.925 0.160 3 185811292 intron variant A/C snv 0.46 0.900 0.963 27 2007 2017
dbSNP: rs7754840
rs7754840
CDKAL1
9 0.807 0.200 6 20661019 intron variant G/A;C;T snv 0.900 0.958 24 2007 2019
dbSNP: rs7901695
rs7901695
TCF7L2
6 0.851 0.160 10 112994329 intron variant T/C snv 0.34 0.900 1.000 23 2006 2020
dbSNP: rs2237895
rs2237895
KCNQ1
10 0.790 0.240 11 2835964 intron variant A/C;T snv 0.900 0.889 18 2008 2019
dbSNP: rs5015480
rs5015480 		9 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 0.900 0.941 17 2007 2019
dbSNP: rs780094
rs780094
GCKR
62 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.900 1.000 17 2007 2018
dbSNP: rs10946398
rs10946398
CDKAL1
7 0.827 0.160 6 20660803 intron variant A/C snv 0.40 0.900 1.000 13 2007 2019
dbSNP: rs2943641
rs2943641 		18 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 0.900 0.923 13 2009 2018
dbSNP: rs864745
rs864745
JAZF1
12 0.763 0.320 7 28140937 intron variant T/C snv 0.41 0.890 0.929 14 2008 2017
dbSNP: rs1387153
rs1387153 		10 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 0.880 1.000 12 2009 2019
dbSNP: rs2237897
rs2237897
KCNQ1
6 0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 0.880 1.000 11 2008 2019
dbSNP: rs4430796
rs4430796
HNF1B
14 0.790 0.280 17 37738049 intron variant A/G snv 0.52 0.870 1.000 11 2009 2019