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: rs1051931
rs1051931
PLA2G7
19 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 0.700 0
dbSNP: rs1805018
rs1805018
PLA2G7
6 0.827 0.200 6 46711566 missense variant A/G snv 6.8E-02 0.10 0.700 0