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: rs7903146
rs7903146
59 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.050 1.000 5 2007 2012
dbSNP: rs1799983
rs1799983
138 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 0.020 1.000 2 2006 2012
dbSNP: rs1801282
rs1801282
77 0.543 0.679 3 12351626 missense variant C/G snp 0.11 1.0E-01 0.020 1.000 2 2006 2018
dbSNP: rs1805192
rs1805192
75 0.545 0.679 3 12379739 missense variant C/G snp 0.020 1.000 2 2006 2018
dbSNP: rs10010131
rs10010131
6 0.821 0.107 4 6291188 intron variant A/G snp 0.66 0.63 0.010 1.000 1 2009 2009
dbSNP: rs1055419
rs1055419
4 0.878 0.071 3 125594988 5 prime UTR variant G/A snp 7.0E-02 0.010 1.000 1 2009 2009
dbSNP: rs11554159
rs11554159
5 0.846 0.179 19 18175134 missense variant G/A snp 0.23 0.24 0.010 1.000 1 2012 2012
dbSNP: rs121909244
rs121909244
7 0.821 0.107 3 12434111 missense variant C/A,T snp 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs1260326
rs1260326
63 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.010 1.000 1 2008 2008
dbSNP: rs137853240
rs137853240
7 0.801 0.071 12 120994405 missense variant G/A snp 0.010 1.000 1 2006 2006
dbSNP: rs1387153
rs1387153
10 0.769 0.250 11 92940662 intergenic variant C/G,T snp 0.33 0.010 1.000 1 2009 2009
dbSNP: rs1558957
rs1558957
3 0.923 0.071 2 162033665 intron variant T/A,C snp 0.67 0.73 0.010 1.000 1 2009 2009
dbSNP: rs17848915
rs17848915
3 0.923 0.071 2 162073469 synonymous variant snp 0.010 1.000 1 2009 2009
dbSNP: rs1800797
rs1800797
16 0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69 0.010 1.000 1 2010 2010
dbSNP: rs193922262
rs193922262
GCK
1 1.000 0.036 7 44145636 stop gained C/A,G snp 4.3E-06 0.010 < 0.001 1 2013 2013
dbSNP: rs193922287
rs193922287
GCK
2 0.923 0.071 7 44153334 missense variant G/A snp 4.0E-06 0.010 < 0.001 1 2013 2013
dbSNP: rs193922289
rs193922289
GCK
5 0.821 0.214 7 44152420 missense variant C/T snp 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs193929375
rs193929375
GCK
5 0.821 0.214 7 44145560 missense variant C/A snp 0.010 1.000 1 2005 2005
dbSNP: rs373269573
rs373269573
2 0.923 0.071 9 137711015 missense variant G/A snp 1.6E-04 3.2E-05 0.010 1.000 1 2002 2002
dbSNP: rs3738435
rs3738435
2 0.923 0.071 1 239907303 intron variant T/C snp 0.24 0.010 < 0.001 1 2011 2011
dbSNP: rs3856806
rs3856806
18 0.715 0.357 3 12434058 synonymous variant C/T snp 0.13 0.13 0.010 1.000 1 2018 2018
dbSNP: rs397514580
rs397514580
1 1.000 0.036 7 44146467 missense variant C/T snp 0.010 1.000 1 2011 2011
dbSNP: rs4402960
rs4402960
12 0.756 0.286 3 185793899 intron variant G/T snp 0.38 0.010 1.000 1 2009 2009
dbSNP: rs4536103
rs4536103
2 0.923 0.071 10 69572448 missense variant A/G snp 0.56 0.55 0.010 1.000 1 2009 2009
dbSNP: rs4994
rs4994
44 0.605 0.536 8 37966280 missense variant A/G snp 0.11 9.0E-02 0.010 1.000 1 2018 2018