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: rs10830963
rs10830963
27 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.800 1.000 11 2009 2019
dbSNP: rs560887
rs560887
18 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.800 1.000 9 2008 2019
dbSNP: rs4607517
rs4607517
GCK
8 0.882 0.080 7 44196069 intron variant G/A;C snv 0.800 1.000 7 2009 2019
dbSNP: rs780094
rs780094
62 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 7 2010 2019
dbSNP: rs11558471
rs11558471
5 1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 0.800 1.000 6 2010 2019
dbSNP: rs10811661
rs10811661
22 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 0.800 1.000 5 2012 2015
dbSNP: rs11708067
rs11708067
9 0.882 0.080 3 123346931 intron variant A/G snv 0.19 0.800 1.000 5 2010 2019
dbSNP: rs1260326
rs1260326
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.800 1.000 5 2012 2019
dbSNP: rs2191349
rs2191349
4 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 0.800 1.000 5 2010 2019
dbSNP: rs7903146
rs7903146
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.800 1.000 5 2009 2019
dbSNP: rs10885122
rs10885122
4 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 0.800 1.000 4 2010 2019
dbSNP: rs11605924
rs11605924
5 1.000 0.080 11 45851540 intron variant A/C snv 0.39 0.800 1.000 4 2010 2019
dbSNP: rs11920090
rs11920090
5 1.000 0.040 3 170999732 intron variant T/A snv 0.20 0.800 1.000 4 2010 2015
dbSNP: rs1387153
rs1387153
10 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 0.800 1.000 4 2009 2019
dbSNP: rs174550
rs174550
13 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 0.800 1.000 4 2010 2015
dbSNP: rs340874
rs340874
7 0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 0.800 1.000 4 2010 2019
dbSNP: rs4506565
rs4506565
22 0.790 0.280 10 112996282 intron variant A/G;T snv 0.800 1.000 4 2010 2019
dbSNP: rs7944584
rs7944584
5 1.000 0.080 11 47314769 intron variant A/T snv 0.19 0.800 1.000 4 2010 2015
dbSNP: rs1483121
rs1483121
4 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 0.800 1.000 3 2012 2019
dbSNP: rs16856247
rs16856247
2 2 168927903 intron variant C/T snv 6.6E-02 0.700 1.000 3 2011 2019
dbSNP: rs1799884
rs1799884
GCK
6 1.000 0.080 7 44189469 intron variant C/T snv 0.17 0.800 1.000 3 2011 2019
dbSNP: rs4841132
rs4841132
14 8 9326086 non coding transcript exon variant A/G snv 0.89 0.700 1.000 3 2012 2015
dbSNP: rs7034200
rs7034200
3 1.000 0.080 9 4289050 intron variant C/A;G snv 0.700 1.000 3 2010 2015
dbSNP: rs895636
rs895636
2 2 44961214 non coding transcript exon variant C/T snv 0.23 0.700 1.000 3 2011 2018
dbSNP: rs10305492
rs10305492
2 1.000 0.080 6 39079018 missense variant G/A snv 1.0E-02 1.1E-02 0.700 1.000 2 2015 2015