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: rs1864400
rs1864400
RET
2 0.925 0.080 10 43114918 intron variant G/A;T snv 0.83 0.700 1.000 1 2014 2014
dbSNP: rs2435357
rs2435357
RET
8 0.790 0.240 10 43086608 intron variant T/C snv 0.79 0.700 1.000 1 2019 2019
dbSNP: rs2505998
rs2505998
RET
2 0.925 0.080 10 43075477 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs2742234
rs2742234
RET
2 0.925 0.080 10 43117161 intron variant C/T snv 0.77 0.700 1.000 1 2009 2009
dbSNP: rs9282834
rs9282834
RET
3 0.882 0.080 10 43111408 missense variant G/A snv 2.3E-03 6.6E-04 0.700 1.000 1 2016 2016