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: rs17133853
rs17133853
DDC ; FIGNL1
1 1.000 0.120 7 50501717 intron variant A/G snv 0.12 0.700 1.000 1 2013 2013