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: rs587777781
rs587777781
SYT2 ; LOC105371686
3 0.925 0.120 1 202599351 missense variant T/G snv 0.800 1.000 1 2014 2014
dbSNP: rs587777782
rs587777782
SYT2 ; LOC105371686
2 0.925 0.040 1 202599348 missense variant G/A snv 0.800 1.000 1 2014 2014