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: rs2046934
rs2046934
P2RY12 ; MED12L
3 0.882 0.200 3 151339854 intron variant G/A;C snv 0.010 1.000 1 2017 2017