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: rs2227924
rs2227924
ATM
3 0.882 0.080 11 108251865 missense variant C/G snv 3.9E-03 1.5E-02 0.010 1.000 1 2003 2003