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: rs7903146
rs7903146
59 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.040 1.000 4 2008 2015
dbSNP: rs2476601
rs2476601
76 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 0.020 1.000 2 2008 2015
dbSNP: rs12571751
rs12571751
2 0.923 0.107 10 79182874 intron variant A/G snp 0.47 0.010 1.000 1 2015 2015
dbSNP: rs231775
rs231775
38 0.608 0.536 2 203867991 missense variant A/G,T snp 0.42; 4.0E-06 0.42 0.010 1.000 1 2015 2015
dbSNP: rs237025
rs237025
20 0.679 0.357 6 149400554 missense variant G/A snp 0.55 0.57 0.010 < 0.001 1 2007 2007
dbSNP: rs689
rs689
6 0.821 0.107 11 2160994 splice region variant A/T snp 0.73 0.62 0.010 1.000 1 2008 2008
dbSNP: rs7961581
rs7961581
6 0.801 0.250 12 71269322 intron variant C/T snp 0.76 0.010 1.000 1 2010 2010
dbSNP: rs8050136
rs8050136
FTO
22 0.744 0.321 16 53782363 intron variant C/A snp 0.40 0.010 1.000 1 2010 2010