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: rs137852561
rs137852561
SYP
1 1.000 X 49191730 missense variant C/G;T snv 0.800 1.000 1 2009 2009
dbSNP: rs139475570
rs139475570
SYP
1 1.000 X 49191502 missense variant C/T snv 1.3E-03 1.2E-03 0.700 1.000 1 2009 2009