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: rs1761667
rs1761667
CD36
12 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.010 1.000 1 2018 2018
dbSNP: rs35874116
rs35874116
TAS1R2
3 1.000 0.040 1 18854899 missense variant T/C snv 0.29 0.31 0.010 1.000 1 2018 2018
dbSNP: rs713598
rs713598
TAS2R38 ; MGAM
7 0.851 0.160 7 141973545 missense variant C/G snv 0.46 0.44 0.010 1.000 1 2018 2018