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: rs2505533
rs2505533
RET
1 1.000 0.080 10 43099005 intron variant T/A;C snv 0.700 1.000 1 2009 2009