Source: ALL
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: rs1801282
rs1801282
77 0.543 0.679 3 12351626 missense variant C/G snp 0.11 1.0E-01 0.100 0.885 26 2000 2013
dbSNP: rs7903146
rs7903146
59 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.100 0.962 26 2006 2018
dbSNP: rs1805192
rs1805192
75 0.545 0.679 3 12379739 missense variant C/G snp 0.100 0.880 25 2000 2012
dbSNP: rs5219
rs5219
14 0.734 0.250 11 17388025 missense variant T/A,C snp 0.64 0.71 0.100 0.900 10 2003 2016
dbSNP: rs9939609
rs9939609
FTO
74 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.100 0.900 10 2009 2018
dbSNP: rs1800562
rs1800562
175 0.463 0.714 6 26092913 missense variant G/A snp 3.3E-02 3.8E-02 0.090 0.667 9 2001 2015
dbSNP: rs1799983
rs1799983
138 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 0.080 0.875 8 2007 2014
dbSNP: rs12255372
rs12255372
20 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.070 1.000 7 2006 2015
dbSNP: rs13266634
rs13266634
13 0.784 0.286 8 117172544 missense variant C/A,T snp 0.29 0.27 0.060 1.000 6 2010 2016
dbSNP: rs137853240
rs137853240
7 0.801 0.071 12 120994405 missense variant G/A snp 0.050 1.000 5 2001 2017
dbSNP: rs1799945
rs1799945
152 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.050 0.800 5 2006 2018
dbSNP: rs137852783
rs137852783
3 0.923 0.071 13 27920364 missense variant G/A,T snp 2.9E-03 2.5E-03 0.040 0.500 4 1999 2005
dbSNP: rs3856806
rs3856806
18 0.715 0.357 3 12434058 synonymous variant C/T snp 0.13 0.13 0.040 1.000 4 2004 2011
dbSNP: rs4880
rs4880
81 0.536 0.643 6 159692840 missense variant A/G snp 0.48 0.47 0.040 0.500 4 2006 2018
dbSNP: rs780094
rs780094
44 0.699 0.286 2 27518370 intron variant T/C snp 0.67 0.040 1.000 4 2010 2013
dbSNP: rs12979860
rs12979860
47 0.608 0.500 19 39248147 intron variant C/T snp 0.38 0.030 0.667 3 2014 2016
dbSNP: rs137852671
rs137852671
9 0.784 0.143 11 17394295 missense variant C/T snp 0.030 1.000 3 2003 2013
dbSNP: rs17107315
rs17107315
32 0.634 0.321 5 147828115 missense variant T/C snp 9.1E-03 8.8E-03 0.030 1.000 3 2002 2005
dbSNP: rs1799883
rs1799883
26 0.679 0.250 4 119320747 missense variant T/A,C,G snp 0.73 0.74 0.030 1.000 3 1999 2010
dbSNP: rs1800206
rs1800206
17 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.030 0.667 3 2005 2007
dbSNP: rs1801278
rs1801278
29 0.652 0.393 2 226795828 missense variant C/G,T snp 4.0E-06; 5.2E-02 6.0E-02 0.030 1.000 3 1999 2009
dbSNP: rs2070600
rs2070600
44 0.602 0.643 6 32183666 missense variant C/T snp 5.3E-02 4.4E-02 0.030 0.667 3 2001 2014
dbSNP: rs2237895
rs2237895
8 0.801 0.179 11 2835964 intron variant A/C,T snp 0.36 0.030 1.000 3 2013 2015
dbSNP: rs2476601
rs2476601
76 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.030 1.000 3 2007 2015
dbSNP: rs4986790
rs4986790
146 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.030 1.000 3 2005 2011