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: rs2281597
rs2281597
CSMD2
1 1.000 0.040 1 33894257 intron variant G/C snv 0.82 0.800 1.000 1 2008 2008