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: rs572115942
rs572115942
7 0.925 0.240 16 30756714 missense variant G/A snv 8.0E-05 7.7E-05 0.700 0
dbSNP: rs953686324
rs953686324
7 0.851 0.160 1 16044506 frameshift variant -/G delins 4.3E-06 5.6E-05 0.700 0
dbSNP: rs11202592
rs11202592
5 0.851 0.200 10 87864461 5 prime UTR variant C/G snv 3.8E-03 1.4E-03 0.010 < 0.001 1 2013 2013
dbSNP: rs13412852
rs13412852
4 0.851 0.120 2 11774815 intron variant C/T snv 0.26 0.010 < 0.001 1 2012 2012
dbSNP: rs193922262
rs193922262
GCK
2 0.925 0.080 7 44145636 stop gained C/A;G snv 4.3E-06 0.010 < 0.001 1 2013 2013
dbSNP: rs193922287
rs193922287
GCK
2 0.925 0.080 7 44153334 missense variant G/A snv 4.0E-06 0.010 < 0.001 1 2013 2013
dbSNP: rs373269573
rs373269573
2 0.925 0.080 9 137711015 missense variant G/A snv 1.6E-04 9.1E-05 0.010 < 0.001 1 2002 2002
dbSNP: rs3738435
rs3738435
2 0.925 0.080 1 239907303 intron variant T/C snv 0.23 0.010 < 0.001 1 2011 2011
dbSNP: rs662
rs662
157 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 < 0.001 1 2006 2006
dbSNP: rs764437500
rs764437500
2 0.925 0.080 9 137716697 missense variant G/A snv 4.0E-06 0.010 < 0.001 1 2002 2002
dbSNP: rs8004664
rs8004664
3 0.925 0.080 14 89568628 intron variant G/A;C snv 0.010 < 0.001 1 2018 2018
dbSNP: rs8066560
rs8066560
2 0.925 0.040 17 17824729 intron variant A/G snv 0.64 0.010 < 0.001 1 2014 2014
dbSNP: rs1085307455
rs1085307455
2 0.925 0.080 7 44149977 missense variant G/A;T snv 8.0E-06 0.700 1.000 12 2000 2012
dbSNP: rs11575937
rs11575937
29 0.653 0.480 1 156136985 missense variant G/A;T snv 0.700 1.000 12 1991 2013
dbSNP: rs1064793998
rs1064793998
GCK
3 0.882 0.080 7 44153325 missense variant C/T snv 0.720 1.000 8 1998 2016
dbSNP: rs776793516
rs776793516
2 0.925 0.080 12 120997492 frameshift variant CA/- delins 4.0E-06 0.700 1.000 7 1997 2014
dbSNP: rs7903146
rs7903146
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.070 1.000 7 2006 2020
dbSNP: rs1375557127
rs1375557127
2 0.925 0.080 20 44424123 missense variant G/A snv 4.0E-06 0.700 1.000 6 2000 2016
dbSNP: rs137853238
rs137853238
6 0.807 0.200 12 120994265 missense variant G/A snv 0.700 1.000 6 1997 2009
dbSNP: rs764232985
rs764232985
GCK
4 0.851 0.080 7 44153381 missense variant C/G;T snv 4.0E-06 0.700 1.000 6 2002 2014
dbSNP: rs1057524900
rs1057524900
GCK
2 0.925 0.080 7 44145173 missense variant G/A;T snv 4.2E-06 0.700 1.000 5 2003 2012
dbSNP: rs1057524907
rs1057524907
2 0.925 0.080 11 2159907 missense variant T/C snv 0.700 1.000 5 2007 2015
dbSNP: rs1564911425
rs1564911425
2 0.925 0.080 11 2159895 missense variant G/C snv 0.700 1.000 5 2007 2015
dbSNP: rs267607555
rs267607555
6 0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 0.700 1.000 5 1990 2013
dbSNP: rs1057524905
rs1057524905
3 0.882 0.080 7 44147834 splice acceptor variant C/T snv 0.700 1.000 4 2003 2009