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: rs5749482
rs5749482
SYN3 ; LOC105373002
3 0.925 0.040 22 32663679 intron variant G/C snv 0.26 0.710 1.000 2 2013 2019