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: rs10246939
rs10246939
TAS2R38 ; MGAM
6 0.851 0.240 7 141972804 missense variant T/C snv 0.49 0.47 0.700 1.000 1 2014 2014
dbSNP: rs1031391
rs1031391
PRH1 ; PRR4 ; TAS2R14 ; PRH1-PRR4 ; PRH1-TAS2R14
1 12 11126493 intron variant C/G snv 0.49 0.700 1.000 1 2014 2014
dbSNP: rs2708377
rs2708377
PRH1 ; PRR4 ; TAS2R14 ; TAS2R46 ; PRH1-PRR4 ; PRH1-TAS2R14
1 12 11063716 intron variant C/A;G;T snv 0.700 1.000 1 2014 2014