Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs770272088
rs770272088
0.882 0.080 7 76302962 missense variant G/A;C;T snv 6.8E-06
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.700 1.000 5 2008 2014