Gene: CHTOP ×
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: rs1300363461
rs1300363461
CHTOP
1 1.000 0.040 1 153645138 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2014 2014