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: rs7138803
rs7138803
17 0.827 0.240 12 49853685 intergenic variant G/A;T snv 0.700 1.000 4 2009 2013
dbSNP: rs17817449
rs17817449
FTO
21 0.716 0.560 16 53779455 intron variant T/A;G snv 0.700 1.000 3 2012 2013
dbSNP: rs12463617
rs12463617
4 1.000 0.080 2 629244 regulatory region variant A/C;T snv 0.700 1.000 2 2013 2014
dbSNP: rs12597579
rs12597579
3 16 20246545 intergenic variant C/A;T snv 0.700 1.000 2 2012 2014
dbSNP: rs13107325
rs13107325
34 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.700 1.000 2 2010 2013
dbSNP: rs2568958
rs2568958
8 0.882 0.160 1 72299433 intron variant G/A;C snv 0.700 1.000 2 2009 2013
dbSNP: rs4771122
rs4771122
4 1.000 0.080 13 27446043 intron variant G/A;C snv 0.700 1.000 2 2010 2013
dbSNP: rs4836133
rs4836133
5 0.925 0.160 5 124996410 intron variant C/A;G;T snv 0.700 1.000 2 2010 2013
dbSNP: rs7498665
rs7498665
9 0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 0.700 1.000 2 2009 2009
dbSNP: rs887912
rs887912
6 1.000 0.080 2 59075742 intron variant T/C;G snv 0.700 1.000 2 2010 2013
dbSNP: rs10458787
rs10458787
4 1.000 0.040 10 4613373 intergenic variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs10789336
rs10789336
3 1 72372723 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs1121980
rs1121980
FTO
18 0.807 0.240 16 53775335 intron variant G/A;C snv 0.700 1.000 1 2008 2008
dbSNP: rs113313252
rs113313252
2 1 74534327 intron variant -/T delins 0.700 1.000 1 2013 2013
dbSNP: rs12617233
rs12617233
2 2 58812863 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs12964056
rs12964056
3 18 60006567 upstream gene variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs13130484
rs13130484
7 1.000 0.080 4 45173674 intergenic variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs13386517
rs13386517
2 2 650479 regulatory region variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs13386627
rs13386627
2 2 650560 regulatory region variant G/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs13388043
rs13388043
2 2 637597 regulatory region variant C/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs13393304
rs13393304
2 2 637830 regulatory region variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs17124318
rs17124318
3 1 63015059 intron variant C/A;G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs201167096
rs201167096
2 1 74534327 intron variant -/T delins 0.700 1.000 1 2013 2013
dbSNP: rs2272903
rs2272903
2 6 50818858 5 prime UTR variant G/A;C snv 0.15 0.700 1.000 1 2013 2013
dbSNP: rs263349
rs263349
2 5 96515920 intron variant T/A;G snv 0.700 1.000 1 2012 2012