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: rs2435357
rs2435357
RET
8 0.790 0.240 10 43086608 intron variant T/C snv 0.79 0.900 0.923 13 2011 2019
dbSNP: rs2506004
rs2506004
RET
3 0.882 0.160 10 43086825 intron variant A/C;T snv 0.050 1.000 5 2011 2015
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: rs1864403
rs1864403
RET
1 1.000 0.080 10 43109502 intron variant A/G snv 0.79 0.700 1.000 1 2009 2009
dbSNP: rs1864410
rs1864410
RET
1 1.000 0.080 10 43080177 intron variant T/G snv 0.80 0.010 1.000 1 2014 2014
dbSNP: rs2435342
rs2435342
RET
1 1.000 0.080 10 43088808 intron variant T/C snv 0.43 0.700 1.000 1 2009 2009
dbSNP: rs2435356
rs2435356
RET
1 1.000 0.080 10 43087702 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2505533
rs2505533
RET
1 1.000 0.080 10 43099005 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs2505538
rs2505538
RET
1 1.000 0.080 10 43095955 intron variant A/G snv 0.38 0.700 1.000 1 2009 2009
dbSNP: rs2506011
rs2506011
RET
1 1.000 0.080 10 43079488 intron variant T/C snv 0.38 0.700 1.000 1 2009 2009
dbSNP: rs2506021
rs2506021
RET
1 1.000 0.080 10 43088700 intron variant C/T snv 0.40 0.700 1.000 1 2009 2009
dbSNP: rs2742234
rs2742234
RET
2 0.925 0.080 10 43117161 intron variant C/T snv 0.77 0.800 1.000 1 2009 2009
dbSNP: rs2742236
rs2742236
RET
1 1.000 0.080 10 43125103 intron variant G/A snv 0.57 0.700 1.000 1 2009 2009
dbSNP: rs3123655
rs3123655
RET
1 1.000 0.080 10 43099746 intron variant C/G snv 0.33 0.700 1.000 1 2009 2009
dbSNP: rs1564489315
rs1564489315
RET
1 1.000 0.080 10 43100496 stop gained G/A snv 0.700 0
dbSNP: rs77316810
rs77316810
RET
10 0.776 0.200 10 43113654 missense variant T/A;C;G snv 0.760 1.000 33 1994 2017
dbSNP: rs76262710
rs76262710
RET
17 0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 0.030 1.000 3 1996 1998
dbSNP: rs77503355
rs77503355
RET
8 0.776 0.160 10 43113655 missense variant G/A;C;T snv 0.730 1.000 3 1998 2009
dbSNP: rs199529397
rs199529397
RET
2 0.925 0.080 10 43109070 missense variant G/A snv 5.6E-05 6.3E-05 0.020 1.000 2 2010 2016
dbSNP: rs377767396
rs377767396
RET
2 0.925 0.080 10 43113623 missense variant C/G;T snv 0.020 0.500 2 1994 1998
dbSNP: rs74799832
rs74799832
RET
33 0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 0.020 1.000 2 1999 2009
dbSNP: rs76397662
rs76397662
RET
4 0.851 0.200 10 43102345 missense variant G/A snv 7.9E-04 2.9E-04 0.020 1.000 2 2010 2016
dbSNP: rs77724903
rs77724903
RET
23 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.720 1.000 2 2009 2013
dbSNP: rs1183365192
rs1183365192
RET
4 0.851 0.160 10 43106550 missense variant C/T snv 7.0E-06 0.010 1.000 1 1997 1997
dbSNP: rs148935214
rs148935214
RET
3 0.882 0.240 10 43114546 missense variant C/T snv 3.2E-04 3.8E-04 0.010 1.000 1 2009 2009