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: rs1038770
rs1038770
SYNPO2
1 1.000 0.080 4 118953332 intron variant G/A snv 9.5E-02 0.010 1.000 1 2013 2013