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: rs121918205
rs121918205
DARS2
1 1.000 0.080 1 173857643 missense variant C/G snv 0.800 1.000 1 2007 2007