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: rs2476601
rs2476601
121 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.030 1.000 3 2008 2019
dbSNP: rs231775
rs231775
115 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs7903146
rs7903146
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.050 1.000 5 2008 2019
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2019 2019
dbSNP: rs5742909
rs5742909
40 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 0.010 1.000 1 2009 2009
dbSNP: rs237025
rs237025
26 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 0.020 1.000 2 2006 2007
dbSNP: rs8050136
rs8050136
FTO
32 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.010 1.000 1 2010 2010
dbSNP: rs689
rs689
9 0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60 0.020 1.000 2 2008 2019
dbSNP: rs7961581
rs7961581
7 0.827 0.200 12 71269322 intron variant C/T snv 0.75 0.010 1.000 1 2010 2010
dbSNP: rs3957146
rs3957146
3 0.882 0.200 6 32713753 upstream gene variant T/C snv 9.1E-02 0.010 1.000 1 2020 2020
dbSNP: rs12571751
rs12571751
2 0.925 0.120 10 79182874 intron variant A/G snv 0.46 0.010 1.000 1 2014 2014
dbSNP: rs231806
rs231806
2 0.925 0.120 2 203844626 intergenic variant C/G;T snv 0.010 1.000 1 2009 2009