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: rs12718541
rs12718541
DDC ; FIGNL1
2 0.925 0.080 7 50482446 intron variant A/G snv 0.55 0.010 1.000 1 2006 2006