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: rs74315507
rs74315507
RAC2
4 0.925 0.080 22 37232857 missense variant C/T snv 0.800 1.000 5 2000 2011
dbSNP: rs1555908409
rs1555908409
RAC2
7 0.851 0.160 22 37232842 missense variant C/T snv 0.700 0