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: rs2420946
rs2420946
4 0.851 0.160 10 121591810 intron variant T/C snv 0.56 0.770 1.000 8 2009 2017
dbSNP: rs28897672
rs28897672
16 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.770 1.000 7 2005 2019
dbSNP: rs10069690
rs10069690
53 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.750 1.000 11 2011 2019
dbSNP: rs10771399
rs10771399
5 0.827 0.080 12 28002147 intergenic variant A/G snv 8.9E-02 0.750 1.000 9 2012 2016
dbSNP: rs2981579
rs2981579
8 0.776 0.280 10 121577821 intron variant A/G snv 0.53 0.740 1.000 9 2009 2017
dbSNP: rs11571833
rs11571833
43 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 0.740 0.875 8 2013 2017
dbSNP: rs1292011
rs1292011
4 0.851 0.080 12 115398717 regulatory region variant A/G snv 0.43 0.740 1.000 7 2012 2017
dbSNP: rs3757318
rs3757318
3 0.882 0.160 6 151592978 intron variant G/A snv 6.1E-02 0.740 1.000 6 2013 2016
dbSNP: rs865686
rs865686
4 0.851 0.080 9 108126198 regulatory region variant G/A;T snv 0.740 1.000 6 2011 2016
dbSNP: rs217727
rs217727
34 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 0.740 0.800 5 2016 2019
dbSNP: rs2180341
rs2180341
3 0.882 0.160 6 127279485 intron variant G/A snv 0.73 0.740 0.800 5 2008 2012
dbSNP: rs2853669
rs2853669
35 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 0.740 0.800 5 2016 2018
dbSNP: rs1011970
rs1011970
22 0.677 0.320 9 22062135 intron variant G/T snv 0.23 0.730 1.000 8 2010 2017
dbSNP: rs2823093
rs2823093
3 0.882 0.080 21 15148511 intergenic variant G/A snv 0.32 0.730 0.833 6 2012 2017
dbSNP: rs1562430
rs1562430
6 0.807 0.160 8 127375606 intron variant T/C snv 0.41 0.730 1.000 5 2010 2015
dbSNP: rs180177132
rs180177132
11 0.790 0.280 16 23621362 stop gained C/T snv 6.0E-05 2.1E-05 0.730 1.000 5 2010 2016
dbSNP: rs4245739
rs4245739
21 0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 0.730 0.800 5 2013 2018
dbSNP: rs16886165
rs16886165
3 0.882 0.160 5 56727256 intergenic variant T/C;G snv 0.22 0.730 1.000 4 2009 2014
dbSNP: rs17530068
rs17530068
3 0.882 0.120 6 81483392 intergenic variant T/C snv 0.19 0.730 1.000 4 2012 2020
dbSNP: rs4442975
rs4442975
7 0.827 0.120 2 217056046 intergenic variant G/T snv 0.47 0.730 1.000 4 2016 2019
dbSNP: rs3734805
rs3734805
2 0.925 0.080 6 151618215 3 prime UTR variant A/C snv 6.9E-02 0.730 1.000 3 2011 2016
dbSNP: rs17817449
rs17817449
FTO
21 0.716 0.560 16 53779455 intron variant T/A;G snv 0.720 1.000 7 2013 2017
dbSNP: rs704010
rs704010
4 0.851 0.080 10 79081391 intron variant T/C snv 0.71 0.720 1.000 6 2010 2017
dbSNP: rs11075995
rs11075995
FTO
5 0.882 0.080 16 53821379 intron variant A/T snv 0.77 0.720 1.000 5 2013 2017
dbSNP: rs1432679
rs1432679
4 0.851 0.080 5 158817075 intron variant C/T snv 0.44 0.720 1.000 5 2013 2017