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: rs121908625
rs121908625
CLTA ; GNE
1 1.000 0.120 9 36219927 missense variant C/T snv 8.0E-06 0.800 1.000 12 2001 2004