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: rs9939609
rs9939609
FTO
74 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.100 0.833 12 2010 2015
dbSNP: rs738409
rs738409
55 0.590 0.536 22 43928847 missense variant C/G snp 0.28 0.22 0.050 1.000 5 2014 2016
dbSNP: rs1137101
rs1137101
41 0.605 0.679 1 65592830 missense variant A/G snp 0.51 0.53 0.040 0.750 4 2001 2011
dbSNP: rs7566605
rs7566605
8 0.801 0.179 2 118078449 intergenic variant C/G snp 0.70 0.040 0.750 4 2008 2016
dbSNP: rs1801282
rs1801282
77 0.543 0.679 3 12351626 missense variant C/G snp 0.11 1.0E-01 0.030 1.000 3 1999 2015
dbSNP: rs1805192
rs1805192
75 0.545 0.679 3 12379739 missense variant C/G snp 0.030 1.000 3 1999 2015
dbSNP: rs5370
rs5370
17 0.715 0.250 6 12296022 missense variant G/T snp 0.23 0.21 0.030 1.000 3 1999 2004
dbSNP: rs1042713
rs1042713
38 0.622 0.571 5 148826877 missense variant G/A snp 0.42 0.43 0.020 1.000 2 2006 2011
dbSNP: rs10830963
rs10830963
17 0.846 0.179 11 92975544 intron variant C/G snp 0.24 0.020 1.000 2 2011 2014
dbSNP: rs1137100
rs1137100
20 0.692 0.464 1 65570758 missense variant A/G snp 0.30 0.28 0.020 0.500 2 2008 2011
dbSNP: rs16147
rs16147
11 0.744 0.286 7 24283791 intergenic variant T/C snp 0.48 0.020 1.000 2 2013 2015
dbSNP: rs17782313
rs17782313
22 0.734 0.250 18 60183864 intergenic variant T/C snp 0.23 0.020 1.000 2 2009 2012
dbSNP: rs2943641
rs2943641
13 0.769 0.143 2 226229029 intergenic variant T/C snp 0.67 0.020 1.000 2 2012 2015
dbSNP: rs324420
rs324420
36 0.657 0.321 1 46405089 missense variant C/A snp 0.24 0.28 0.020 0.500 2 2005 2007
dbSNP: rs4402960
rs4402960
12 0.756 0.286 3 185793899 intron variant G/T snp 0.38 0.020 1.000 2 2015 2015
dbSNP: rs4986938
rs4986938
23 0.657 0.536 14 64233098 3 prime UTR variant C/T snp 0.31 0.32 0.020 1.000 2 2009 2013
dbSNP: rs56149945
rs56149945
35 0.626 0.643 5 143399752 missense variant T/A,C snp 2.0E-02 2.2E-02 0.020 1.000 2 2003 2003
dbSNP: rs696217
rs696217
24 0.685 0.536 3 10289773 missense variant G/T snp 8.8E-02 7.2E-02 0.020 1.000 2 2004 2007
dbSNP: rs8050136
rs8050136
FTO
22 0.744 0.321 16 53782363 intron variant C/A snp 0.40 0.020 0.500 2 2011 2013
dbSNP: rs10128072
rs10128072
1 1 65491413 intron variant A/C snp 0.18 0.010 1.000 1 2012 2012
dbSNP: rs1016862
rs1016862
2 1.000 0.036 18 60371844 missense variant A/C snp 0.010 1.000 1 2009 2009
dbSNP: rs1042571
rs1042571
4 0.878 0.107 2 25161018 3 prime UTR variant G/A snp 0.15 0.010 1.000 1 2013 2013
dbSNP: rs1042615
rs1042615
3 1.000 0.036 12 63150429 missense variant A/C,G,T snp 0.60; 1.2E-05 0.64 0.010 1.000 1 2009 2009
dbSNP: rs1042714
rs1042714
38 0.634 0.464 5 148826910 stop gained G/C,T snp 0.68 0.67 0.010 1.000 1 2006 2006
dbSNP: rs1044925
rs1044925
2 1.000 0.071 1 179354603 3 prime UTR variant C/A,G snp 0.67; 3.2E-05 0.010 1.000 1 2015 2015