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: rs1201607264
rs1201607264
TAS2R38 ; MGAM
1 7 141973254 missense variant C/A snv 7.0E-06 0.010 1.000 1 2012 2012
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 2012 2012