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: rs77600076
rs77600076
CHODL
1 1.000 0.040 21 18159125 intron variant A/C snv 2.5E-02 0.800 1.000 1 2013 2013