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: rs2042329
rs2042329
CWC27
3 0.882 0.120 5 64771925 intron variant T/C;G snv 0.710 1.000 1 2016 2016