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: rs200703101
rs200703101
1 19 44908757 missense variant G/C,T snp 0.700 1 2015 2015
dbSNP: rs11575937
rs11575937
17 0.715 0.321 1 156136985 missense variant G/A,T snp 0.020 1.000 2 2001 2001
dbSNP: rs1260326
rs1260326
63 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.020 1.000 2 2008 2009
dbSNP: rs1799883
rs1799883
26 0.679 0.250 4 119320747 missense variant T/A,C,G snp 0.73 0.74 0.020 1.000 2 2005 2010
dbSNP: rs1800206
rs1800206
17 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.020 0.500 2 2004 2007
dbSNP: rs3135506
rs3135506
17 0.734 0.214 11 116791691 missense variant G/A,C snp 3.0E-05; 6.8E-02 9.6E-05; 6.1E-02 0.020 1.000 2 2008 2008
dbSNP: rs780094
rs780094
44 0.699 0.286 2 27518370 intron variant T/C snp 0.67 0.020 1.000 2 2008 2009
dbSNP: rs80356814
rs80356814
16 0.724 0.321 1 156138697 synonymous variant C/T snp 8.0E-06 3.2E-05 0.020 0.500 2 2002 2005
dbSNP: rs11542035
rs11542035
1 19 44908706 missense variant G/A snp 1.9E-05 3.2E-05 0.010 1.000 1 1995 1995
dbSNP: rs11868035
rs11868035
10 0.801 0.179 17 17811787 splice region variant G/A snp 0.45 0.34 0.010 1.000 1 2009 2009
dbSNP: rs1217691063
rs1217691063
29 0.652 0.571 1 11796309 missense variant A/G snp 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs12363280
rs12363280
1 11 231980 intron variant C/A,G snp 3.5E-05; 0.17 0.010 1.000 1 2016 2016
dbSNP: rs13266634
rs13266634
13 0.784 0.286 8 117172544 missense variant C/A,T snp 0.29 0.27 0.010 1.000 1 2015 2015
dbSNP: rs137852912
rs137852912
10 0.784 0.107 1 55057454 missense variant G/A,C,T snp 7.2E-05 6.4E-05 0.010 1.000 1 2006 2006
dbSNP: rs1430583
rs1430583
1 4 140565830 intron variant C/T snp 4.3E-03; 0.19 0.010 1.000 1 2016 2016
dbSNP: rs1685354
rs1685354
1 11 74002546 intron variant A/G snp 0.29 0.010 1.000 1 2016 2016
dbSNP: rs17465637
rs17465637
10 0.784 0.143 1 222650187 intron variant A/C,G,T snp 0.64; 6.4E-06 0.59 0.010 < 0.001 1 2012 2012
dbSNP: rs1746661
rs1746661
3 0.923 0.071 1 32869438 intron variant G/A,T snp 0.15 0.010 < 0.001 1 2015 2015
dbSNP: rs1799884
rs1799884
GCK
4 1.000 0.071 7 44189469 intron variant C/T snp 0.16 0.010 1.000 1 2009 2009
dbSNP: rs1800795
rs1800795
58 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2016 2016
dbSNP: rs1801282
rs1801282
77 0.543 0.679 3 12351626 missense variant C/G snp 0.11 1.0E-01 0.010 1.000 1 2001 2001
dbSNP: rs1805192
rs1805192
75 0.545 0.679 3 12379739 missense variant C/G snp 0.010 1.000 1 2001 2001
dbSNP: rs1984112
rs1984112
2 1.000 0.036 7 80613604 intron variant A/G snp 0.33 0.010 1.000 1 2013 2013
dbSNP: rs201058276
rs201058276
F7
17 0.724 0.214 13 113118731 missense variant G/A,C snp 4.8E-05; 4.0E-06 9.6E-05 0.010 1.000 1 1998 1998
dbSNP: rs2016520
rs2016520
4 0.923 0.107 6 35411001 5 prime UTR variant C/T snp 0.79 0.010 1.000 1 2010 2010