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: rs1057518775
rs1057518775
4 0.851 0.160 11 17387907 missense variant G/A;C snv 0.700 0
dbSNP: rs1344172059
rs1344172059
12 0.882 0.080 11 17430838 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs141322087
rs141322087
13 0.851 0.160 11 17404552 missense variant C/T snv 1.2E-05 2.1E-05 0.700 0
dbSNP: rs146036912
rs146036912
2 0.925 0.080 4 108027727 missense variant T/C snv 6.8E-05 9.8E-05 0.700 0
dbSNP: rs146539065
rs146539065
34 0.752 0.240 4 25145092 synonymous variant C/T snv 2.8E-05 4.2E-05 0.700 0
dbSNP: rs1801175
rs1801175
8 0.807 0.240 17 42903947 missense variant C/T snv 5.7E-04 3.4E-04 0.700 0
dbSNP: rs587782995
rs587782995
42 0.708 0.360 5 140114480 missense variant T/C snv 0.700 0
dbSNP: rs763028380
rs763028380
12 0.851 0.320 11 17453271 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 0.700 0
dbSNP: rs776969714
rs776969714
34 0.752 0.240 4 25145129 splice acceptor variant -/C delins 4.2E-05 0.700 0
dbSNP: rs869025222
rs869025222
9 0.827 0.240 3 25580574 missense variant T/C snv 0.700 0
dbSNP: rs886039469
rs886039469
35 0.701 0.560 10 76891709 missense variant T/C snv 0.700 0
dbSNP: rs1799821
rs1799821
8 0.827 0.200 1 53210776 missense variant G/A snv 0.49 0.46 0.010 1.000 1 1992 1992
dbSNP: rs1799822
rs1799822
4 0.925 0.080 1 53213557 missense variant A/G snv 0.16 0.15 0.010 1.000 1 1992 1992
dbSNP: rs74315293
rs74315293
5 0.851 0.200 1 53213509 missense variant C/T snv 2.4E-05 1.4E-05 0.010 1.000 1 1992 1992
dbSNP: rs121434278
rs121434278
3 0.882 0.120 1 75740094 missense variant G/A snv 4.0E-05 7.0E-05 0.010 1.000 1 1994 1994
dbSNP: rs373345919
rs373345919
5 0.882 0.080 17 42909364 stop gained C/T snv 2.8E-05 2.8E-05 0.010 1.000 1 2000 2000
dbSNP: rs1799958
rs1799958
4 0.882 0.160 12 120738280 missense variant G/A snv 0.26 0.21 0.010 1.000 1 2002 2002
dbSNP: rs28936375
rs28936375
15 0.752 0.320 1 53197092 missense variant C/A snv 1.7E-04 2.2E-04 0.010 1.000 1 2002 2002
dbSNP: rs1208845035
rs1208845035
GCK
1 1.000 0.040 7 44145270 missense variant G/A snv 0.010 1.000 1 2003 2003
dbSNP: rs112445441
rs112445441
32 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2005 2005
dbSNP: rs1383147053
rs1383147053
DLD
4 0.882 0.120 7 107901762 missense variant G/A snv 0.010 1.000 1 2005 2005
dbSNP: rs137852671
rs137852671
10 0.790 0.160 11 17394295 missense variant C/T snv 0.010 1.000 1 2010 2010
dbSNP: rs1042713
rs1042713
63 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.020 1.000 2 2008 2011
dbSNP: rs137853238
rs137853238
6 0.807 0.200 12 120994265 missense variant G/A snv 0.020 1.000 2 2011 2011
dbSNP: rs121918188
rs121918188
2 0.925 0.080 9 94609998 missense variant C/T snv 2.4E-05 7.0E-06 0.010 1.000 1 2011 2011