Source: ALL
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: rs121918214
rs121918214
FTO
3 1.000 0.200 16 53873837 missense variant G/A snv 4.0E-06 7.0E-06 0.800 1.000 4 2009 2016
dbSNP: rs781028867
rs781028867
FTO
3 1.000 0.200 16 53873846 missense variant C/A;T snv 4.0E-06 0.800 1.000 4 2009 2016
dbSNP: rs1410999299
rs1410999299
FTO
1 1.000 0.200 16 53826003 missense variant A/G snv 1.6E-05 0.700 0
dbSNP: rs745616565
rs745616565
FTO
3 1.000 0.200 16 53873855 missense variant G/A snv 1.6E-05 2.1E-05 0.700 0