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: rs75076352
rs75076352
RET
24 0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 0.060 1.000 6 1998 2015
dbSNP: rs75996173
rs75996173
RET
21 0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 0.050 1.000 5 1998 2015
dbSNP: rs377767404
rs377767404
RET
11 0.742 0.160 10 43114488 missense variant T/C snv 0.010 1.000 1 2005 2005
dbSNP: rs78014899
rs78014899
RET
12 0.742 0.160 10 43118392 missense variant G/A;C;T snv 8.0E-06 0.010 < 0.001 1 2006 2006